Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30493Generated: October 25, 2026

2-Oxobutanoic Acid → 2-oxo-butyric acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester

https://huagongshe.com/reaction/30493

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Oxobutanoic AcidHCID 58—
Reactant(+)-8-PhenylmentholHCID 577105—
Catalystp-Toluenesulfonic acid monohydrateHCID 521998—
SolventBenzeneHCID 241—
Product2-oxo-butyric acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl esterHCID 1108839692.5%

Reaction Steps

A solution of 2.28 g 2-oxobutyric acid (2, 22.11 mmol, 1.3 eq), 4.04 g (−)-8-phenylmenthol (18, 17.02 mmol, 1.0 eq) and 169.9 mg para-toluenesulfonic acid monohydrate (0.884 mmol, 0.52 eq) in 48 mL benzene was heated to reflux for 20 h 35 min. After cooling down to room temperature, the solution was washed twice with 50 mL saturated aqueous sodium hydrogencarbonate solution, and subsequently with 50 mL water and 50 mL brine. The organic phase was dried over 5 g sodium sulfate and was filtered. The filter cake was washed with 10 mL benzene. The organic phase was evaporated to dryness in a rotary evaporator (40° C., 20 mbar) yielding the title compound (4.98 g, 92% by weight) as colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07423152B2
Source datasetuspto-grants-2008_09
ORD IDord-e0866e356d694e0da29bc5cae5ef3ed2
Source noteuspto-grants-2008_09