Metal-catalyzed C–H borylation reactions are transition metal catalyzed organic reactions that produce an organoboron compound through functionalization of
aliphatic and
aromatic C–H bonds and are therefore useful reactions for
carbon–hydrogen bond activation.
[1] Metal-catalyzed C–H borylation reactions utilize transition metals to directly convert a C–H bond into a C–B bond. This route can be advantageous compared to traditional borylation reactions by making use of cheap and abundant hydrocarbon starting material, limiting prefunctionalized organic compounds, reducing toxic byproducts, and streamlining the synthesis of biologically important molecules.
[2][3] Boronic acids, and boronic esters are common boryl groups incorporated into organic molecules through borylation reactions.
[4] Boronic acids are trivalent boron-containing organic compounds that possess one alkyl substituent and two hydroxyl groups. Similarly, boronic esters possess one alkyl substituent and two ester groups. Boronic acids and esters are classified depending on the type of carbon group (R) directly bonded to boron, for example alkyl-, alkenyl-, alkynyl-, and aryl-boronic esters. The most common type of starting materials that incorporate boronic esters into organic compounds for transition-metal catalyzed borylation reactions have the general formula (RO)
2B-B(OR)
2. For example,
Bis(pinacolato)diboron (B
2Pin
2), and bis(catecholato)diborane (B
2Cat
2) are common boron sources of this general formula.
[5]
The boron atom of a boronic ester or acid is sp
2 hybridized possessing a vacant p orbital, enabling these groups to act as
Lewis acids. The C–B bond of boronic acids and esters are slightly longer than typical C–C single bonds with a range of 1.55-1.59 Å. The lengthened C–B bond relative to the C–C bond results in a bond energy that is also slightly less than that of C–C bonds (323 kJ/mol for C–B vs 358 kJ/mol for C–C).
[6] The
carbon–hydrogen bond has a bond length of about 1.09 Å, and a bond energy of about 413 kJ/mol. The C–B bond is therefore a useful intermediate as a bond that replaces a typically unreactive C–H bond.
Organoboron compounds are organic compounds containing a carbon-boron bond. Organoboron compounds have broad applications for chemical synthesis because the C–B bond can easily be converted into a C–X (X = Br, Cl), C–O, C–N, or C–C bond. Because of the versatility of the C–B bond numerous processes have been developed to incorporate them into organic compounds.
[7] Organoboron compounds are
traditionally synthesized from
grignard reagents through
hydroboration, or diboration reactions.
[8]
Synthetically important aryl and alkenyl boron compounds can be synthesized from the corresponding halides using transition metal catalysts. Pinachol diborane is used commonly as the boron source due to stability, easy handling, and wide commercial availability.
In recent years, iridium- and rhodium-catalyzed direct C-H borylationreactions that do not require halogenated precursors have been reported.
The iridium-catalyzed systems are sensitive to steric influences and occasionally allow for meta-functionalization, which is difficult by conventional lithiation and electrophilic substitution approaches.
・Ishiyama, T.; Murata, M.; Miyaura, N.
J. Org. Chem. 1995,
60, 7508. DOI:
10.1021/jo00128a024
・Ishiyama, T.; Takagi, J.; Ishida, K.; Miyaura, N.; Anastasi, N. R.; Hartwig, J. F.
J. Am. Chem. Soc. 2002,
124,
390. DOI:
10.1021/ja0173019
・Takagi, J.; Takahashi, K.; Ishiyama, T.; Miyaura, N.
J. Am. Chem. Soc. 2002,
124, 8001. DOI:
10.1021/ja0202255
・Ishiyama, T.; Takagi, J.; Hartwig, J. F.; Miyaura, N.
Angew. Chem. Int. Ed. 2002,
41, 3056.
[abstract]
Reaction Mechanism
Examples
The β-selective C-H borylation of porphyrin.
The rhodium-catalyzed functionalization of unreactive alkanes at terminal position.
[1A]Chen, H.; Schlecht, S.; Semple, T. C.; Hartwig, J. F.
Science 2000,
287, 1995. doi:
10.1126/science.287.5460.1995
Borylation of aryl bromide.
[2A]Ishiyama, T.; Murata, M.; Miyaura, N.
J. Org. Chem. 1995,
60, 7508. DOI:
10.1021/jo00128a024
KOAc is the base of choice. Stronger bases like K2CO3 and K3PO4 increases the risk of dimerization via the Suzuki coupling.
The order of reaction rate in different solvents is: DMSO >> DMF > 1,4-dioxane.
[1A] Chen, H.; Schlecht, S.; Semple, T. C.; Hartwig, J. F.
Science 2000,
287, 1995. doi:
10.1126/science.287.5460.1995
[2A] Ishiyama, T.; Murata, M.; Miyaura, N.
J. Org. Chem. 1995,
60, 7508. DOI:
10.1021/jo00128a024
Metal-catalyzed C–H borylation reactions
Alkanes can be selectively borylated at the primary C–H bond using rhodium catalysts.
[9] Notably, selectivity for the primary C–H bond is exclusive even in the presence of heteroatoms in the carbon-hydrogen chain. The rhodium-catalyzed borylation of methyl C–H bonds occurs selectively without a dependence on the position of the heteroatom. Borylation occurs selectively at the least sterically hindered and least electron rich primary C–H bond in a range of
acetals,
ethers,
amines, and alkyl fluorides.
[10] Additionally, no reaction is shown to occur in the absence of primary C–H bonds, for example when
cyclohexane is the substrate.
Selective functionalization of a primary alkane bond is due to the formation of a kinetically and thermodynamically favorable primary alkyl-metal complex over formation of a secondary alkyl-metal complex.
[11]
Primary versus secondary metal-alkyl complex
The greater stability of primary versus secondary alkyl complexes can be attributed to several factors. First, the primary alkyl complex is favored sterically over the secondary alkyl complex. Second, partial negative charges are often present on the α-carbon of a metal-alkyl complex and a primary alkyl ligand supports a partial negative charge better than a secondary alkyl ligand. The origin of selectivity for aliphatic C–H borylation using rhodium catalysts was probed using a type of mechanistic study called
hydrogen–deuterium exchange. H/D exchanged showed that regioselectivity of the overall process shown below results from selective cleavage of primary over secondary C–H bonds and selective functionalization of the primary metal-alkyl intermediate over the secondary metal-alkyl intermediate.
[12]
The synthetic utility of aliphatic C–H borylation has been applied to the modification of polymers through borylation followed by oxidation to form hydroxyl-capped polymers.
[13]
Aromatic C–H borylation
Steric directed C–H borylation of arenes
Aromatic C–H borylation was developed by Hartwig and Ishiyama using the diboron reagent
Bis(pinacolato)diboron catalyzed by 4,4’-di-tert-butylbipyridine (dtbpy) and [Ir(COD)(OMe)]
2.
[14] With this catalyst system the borylation of aromatic C–H bonds occurs with regioselectivity that is controlled by
steric effects of the starting arene. The selectivity for functionalization of aromatic C–H bonds is governed by the general rule that the reaction does not occur
ortho to a substituent when a C–H bond lacking an
ortho substituent is available.
[11] When only one functional group is present borylation occurs in the
meta and
para position in statistical ratios of 2:1 (meta:para). The
ortho isomer is not detected due to the steric effects of the substituent.
[15]
Addition of Bpin occurs in only one position for symmetrically substituted 1,2- and 1,4-substituted arenes. Symmetrical or unsymmetrical 1,3-substituted arenes are also selectively borylated because only one C–H bond is sterically accessible.
The synthetic importance of aromatic C–H borylation is shown below, where a 1,3-disubstited aromatic compound can be directly converted to a 1,3,5-organoborane compound and subsequently functionalized.
[14]
C–H borylation of heteroarenes
Heteroarenes can also undergo borylation under iridium-catalyzed conditions, however, site-selectivity in this case is controlled by
electronic effects, where
furans,
pyroles, and
thiophenes undergo reaction at the C–H bond alpha to the heteroatom. In this case selectivity is suggested to occur through the C–H bond alpha the to heteroatom because it is the most acidic C–H bond and therefore the most reactive.
[11]
Directed ortho C–H borylation
Using the same catalyst system directing groups can be employed to achieve regioselectivity without substituents as steric mediators. For example Boebel and Hartwig reported a method to conduct
ortho-borylation where a dimethyl-hydrosilyl directing group on the arene undergoes iridium catalyzed borylation at the C–H bond
ortho to the
silane directing group.
[18] Selectivity for the
ortho position in the case of using hydrosilyl directing groups has been attributed to reversible addition of the Si-H bond to the metal center, leading to preferential cleavage of the C–H bond
ortho to the hydrosilyl substituent. Several other strategies to achieve
ortho-borylation of arenes have been developed using various directing groups.
[19][20][21]
Mechanistic detail for the C–H borlyation of arenes
A trisboryl iridium complex has been proposed to facilitate the mechanism for each of these reactions that result in C–H borylation of arenes and heteroarenes.
Kinetic studiesand
isotopic labelling studies have revealed that an Ir(III) triboryl complex reacts with the arene in the catalytic process.
[22] A version of the catalytic cycle is shown below for the
ortho borylation of hydrosilane compounds. Kinetic data show that an observed trisboryl complex coordinated to
cyclooctene rapidly and reversibly dissociates cyclooctene to form a 16 electron trisboryl complex. In the case of using benzyldimethylsilane as a directing group it is proposed that benzyldimethylsilane reacts with the trisboryl iridium catalyst through reversible addition of the Si-H bond to the metal center, followed by selective
ortho-C–H bond activation via
oxidative addition and
reductive elimination.
[23]
The application of organoboron compounds in organic synthesis.
Organoboron derivatives as synthetic intermediates are an important class of compounds in
organic synthesis. They have been common utilized in several asymmetric reduction reactions to synthesize chiral
alcohols or in coupling reactions to form carbon-carbon bond, carbon-nitrogen bond or carbon-oxygen bond.
[24][25][26]
Reduction reactions with organoboron compounds
In 1981, Hirao and co-workers have found that asymmetric reduction of prochiral armomatic ketones with
chiral amino
alcohols and
borane afforded the corresponding secondary alcohols with 60%
ee. They found out that the chiral amino
alcohols would react with
borane to form aloxyl-amine-borane complexes. The complexes are proposed to contain a relatively rigid five member-ring system which makes them thermal and hydrolytic stable and soluble in a wide variety of
protic and aprotic solvents.
[27]
In 1987,
E. J. Corey and co-workers found out that the formation of oxazaborolidines from borane and
chiral amino
alcohols. And the oxazaborolidines were found to catalyze the rapid and highly enantioselective reduction of prochiral ketones in the presence of BH3THF. This enantioselective reduction of achiral
ketones with catalytic oxazaborolidine is called Corey–Bakshi–Shibata reduction or CBS reduction.
[28][29]
In 1977, M. M. Midland and co-workers reported a surprising observation that B-3-alpha-Pinanyl-9-borabicyclo [3,3,1] nonane, readily prepared by hydroboration of (+)-alpha-pinene with
9-borobicyclo[3,3,1] nonane, rapidly reduces benzaldehyde-alpha-d to (S)-(+)-benzyl-alpha-d alcohol with an essentially quantitative asymmetric induction.
[30]
In the same year, M. M. Midland discovered B-3-alpha-pinanyl-9-BBN as the reducing agent, which could be easily available by reacting (+)-alpha-pinene with 9-BBN. The new reducing agent was later commercialized by
Aldrich Co. under the name
Alpine Borane and the asymmetric reduction of carbonyl groups with either enantiomer of Alpine-Borane is known as Midland Alpine-Borane reduction.
[31]
In 2012, U. R. Y. Venkateswarlu and co-workers have reported a stereoselective method to synthesize pectinolide H. Midland reduction and Sharpless dihydroxylation reaction are involved in generating the three chiral centers at C–4’, C–5 and C–1’.
[32]
Coupling reactions with organoboron compounds
In 1993, N. A. Petasis and I. Akrltopoulou reported an efficient synthesis of allylic amines with a modified
Mannich reaction. In this modified
Mannich reaction, they have found that vinyl boronic acids can participate as
nucleophiles to give geometrically pure allylamines .This modified
Mannich reaction was known as Petasis boronic acid-Mannich Reaction.
[33][34]
Roush asymmetric allylation
In 1978, R. W. Hoffmann and T. Herold reported on the enantioselective synthesis of secondary homoallyl alcohols via chiral non-racemic allylboronic
esters. The homoallylic alcohols were formed with excellent
yield and moderate enantioselectivity.
[35]
In 1985, W. R. Roush and co-workers found out that tartrate modified allylic boronates offer a simple, highly attractive approach to the control of facial selectivity in reactions with chiral and achiral aldehydes. In the following years, W.R. Roush and co-workers extended this strategy to the synthesis of 2-Butene-1,4-Diols and Anti-Diols. This kind of reaction is known as Rouch asymmetric allylation.
[36][37][38][39]
In 2011, R. A. Fernandes and P. Kattanguru have completed an improved total synthesis of (8S, 11R, 12R)- and (8R, 11R, 12R)-topsentolide B2 diastereomers in eight steps. In the paper, diastereoselective Roush allylation reaction was used as a key reaction in the total syntheis to introduce two chiral intermediate. And then the authors synthesized the two diastereomers through these two chiral intermediates.
[40]
In 1979, N. Miyaura and A. Suzuki reported the synthesis of arylated (E)-alkenes in high yield from
aryl halides with alkyl-1-enylboranes and catalyzed by tetrakis(
triphenylphosphine)palladium and bases. Then A. Suzuki and co-workers extend this kind of reaction to other organoboron compounds and other alkenyl,
aryl, alkyl halides and
triflate. The palladium-catalyzed cross-coupling reaction organoboron compounds and these organic halides to form carbon-carbon bonds are known as
Suzuki–Miyaura Cross-Coupling.
[41][42]
In 2013, Joachim Podlech and co-workers determined the structure of Alternaria mycotoxin altenuic acid III by NMR spectroscopic analysis and completed its total synthesis. In the synthetic strategy, Suzuki-Miyaura Cross-Coupling reaction was used with a highly functionalized boronate and butenolides to synthesize a precursor of the natural product in high yield.
[43]
Modified Ullmann biaryl ether and biaryl amine synthesis
In 1904,
Fritz Ullmann found out that copper powder could significantly improve the reaction of aryl halides with phenols to give biaryl ethers. This reaction is known as
Ullmann condensation. In 1906, I. Goldberg extended this reaction to synthesize an arylamine by reacting aryl halides with an amide in the presence of Potassium Carbonate and CuI. This reaction is known as Goldberg modified Ullmann condensation.
[44] In 2003, R. A. Batey and T. D. Quach have modified this kind of reactions by using potassium
organotrifluoroborates salts to react with aliphatic alcohols, aliphatic amines or anilines to synthesize aryl ethers or aryl amines.
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