Homobenzotetramisole (HBTM): A General Organocatalyst for Asymmetric Acylations


We are proud to offer the isothiourea organocatalyst homobenzotetramisole (HBTM) as part of our asymmetric catalysis portfolio in both (R) and (S) enantiomeric forms. These compounds have found broad applications in enantioselective transformations and kinetic resolutions of a variety of functional groups with low catalyst loadings.


Representative Transformations

Kinetic Resolutions

S-HBTM was originally developed by Birman and coworkers for use in kinetic resolutions of secondary alcohols as an alternative to enzymatic conditions.1 Selectivity factors of up to 122 are reported. The HBTM catalyst has been used in kinetic resolutions of allylic, propargylic, and benzylic secondary alcohols with a variety of organic solvents across a range of temperatures. Reactions are typically complete within a few hours. Optimal conditions were reported at lower temperatures (0 to –55 °C) in toluene, chloroform, or tert-amyl alcohol.1,2

toluene, chloroform, or tert-amyl alcohol

HBTM is useful in the kinetic resolution of a-arylalkanoic acids, a-aryloxy-alkanoic acids, α-alkoxy-alkanoic acids, α-haloalkanoic acids, and protected α-amino acids.3,4 Selectivity factors of up to 96 are reported. This transformation typically utilizes toluene as the solvent at low temperature over 24 hours.

solvent at low temperature over 24 hours

A dynamic kinetic resolution has been reported with HBTM for the formation of enantioenriched α-thioalkanoic acids.4,5 This process occurs with a broad substrate scope to produce high yields and high enantiopurities.

high yields and high enantiopurities

Enantioselective Transformations

HBTM has been used for enantioselective carboxyl group transfer of oxazolyl carbonates.6 This process typically occurs in dichloromethane at low temperature for 16 hours to give high yields and high enantiopurities for a variety of substrates.

enantioselective carboxyl group transfer of oxazolyl carbonates

HBTM has been used for an enantioselective nucleophile-catalyzed, Michael-aldol-β-lactonization (NCMAL) sequence.7 This process occurs in tetrahydrofuran/dichloromethane over ≤ 24 h to give products with high diastereomeric ratios, high yields, and high enantiopurities.

enantioselective nucleophile-catalyzed

Determination of Absolute Configuration

HBTM is the catalyst of choice for the Competing Enantioselective Conversion (CEC) method, which is used to assign the absolute configuration of enantioenriched stereocenters. The CEC method with HBTM has been reported for secondary alcohols, where reaction conversion is measured by 1H NMR8 and TLC.9 The TLC analysis has also been converted into an undergraduate laboratory experiment.10 This process occurs at room temperature, with the duration ranging from 30 min to a few hours.

Competing Enantioselective Conversion (CEC) method

The following mnemonic is used to identify the absolute configuration of secondary alcohols using the R-HBTM and S-HBTM catalysts.8-10

R-HBTM and S-HBTM catalysts.

The CEC method with HBTM has also been reported to determine the absolute configuration of oxazolidinones, lactams, and thiolactams.11 This process is typically complete after a few hours at room temperature or 50 °C. The following mnemonic is used to identify the absolute configuration of these systems using the R-HBTM and S-HBTM catalysts.

R-HBTM and S-HBTM catalysts

Additional Studies

The nucleophilicity and Lewis basicity of HBTM have been studied based on rate and equilibrium constants from a series of experiments with benzhydrylium ions.12 Additionally, a detailed kinetic analysis of the HBTM-catalyzed esterification of secondary alcohols has also been conducted, which offers insight into the catalytic cycle for this transformation.13

Special thanks to Mr. Alex Wagner and Prof. Scott Rychnovsky for contributing this technology spotlight.



Purification of Basic Compounds with Functionalized SilicaGel. Synfacts. 2008(10):1115-1115. http://dx.doi.org/10.1055/s-2008-1078198
Li X, Jiang H, Uffman EW, Guo L, Zhang Y, Yang X, Birman VB. 2012. Kinetic Resolution of Secondary Alcohols Using Amidine-Based Catalysts. J. Org. Chem.. 77(4):1722-1737. http://dx.doi.org/10.1021/jo202220x
Yang X, Birman V. 2009. Homobenzotetramisole-Catalyzed Kinetic Resolution of ?-Aryl-, ?-Aryloxy-, and ?-Arylthioalkanoic Acids. Adv. Synth. Catal.. 351(14-15):2301-2304. http://dx.doi.org/10.1002/adsc.200900451
Yang X, Birman VB. 2011. Chem.–Eur. J.. 17, 11296.
Yang X, Birman VB. 2011. Nonenzymatic Dynamic Kinetic Resolution of ?-(Arylthio)- and ?-(Alkylthio)alkanoic Acids. Angew. Chem. Int. Ed.. 50(24):5553-5555. http://dx.doi.org/10.1002/anie.201007860
Joannesse C, Johnston C, Concellón C, Simal C, Philp D, Smith A. 2009. Isothiourea-Catalyzed Enantioselective Carboxy Group Transfer. Angewandte Chemie International Edition. 48(47):8914-8918. http://dx.doi.org/10.1002/anie.200904333
Liu G, Shirley ME, Van KN, McFarlin RL, Romo D. 2013. Rapid assembly of complex cyclopentanes employing chiral, ?,?-unsaturated acylammonium intermediates. Nature Chem. 5(12):1049-1057. http://dx.doi.org/10.1038/nchem.1788
Wagner AJ, David JG, Rychnovsky SD. 2011. Determination of Absolute Configuration Using Kinetic Resolution Catalysts. Org. Lett.. 13(16):4470-4473. http://dx.doi.org/10.1021/ol201902y
Wagner AJ, Rychnovsky SD. 2013. Determination of Absolute Configuration of Secondary Alcohols Using Thin-Layer Chromatography. J. Org. Chem.. 78(9):4594-4598. http://dx.doi.org/10.1021/jo400432q
Wagner AJ, Miller SM, Nguyen S, Lee GY, Rychnovsky SD, Link RD. 2013. J. Chem. Educ. in press..
Perry MA, Trinidad JV, Rychnovsky SD. 2013. Absolute Configuration of Lactams and Oxazolidinones Using Kinetic Resolution Catalysts. Org. Lett.. 15(3):472-475. http://dx.doi.org/10.1021/ol303239t
Maji B, Joannesse C, Nigst TA, Smith AD, Mayr H. 2011. Nucleophilicities and Lewis Basicities of Isothiourea Derivatives. J. Org. Chem.. 76(12):5104-5112. http://dx.doi.org/10.1021/jo200803x
Wagner AJ, Rychnovsky SD. 2013. Kinetic Analysis of the HBTM-Catalyzed Esterification of an Enantiopure Secondary Alcohol. Org. Lett.. 15(21):5504-5507. http://dx.doi.org/10.1021/ol402643n