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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 603321Generated: October 25, 2026

Pyridine → (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl (E)-3-(3,4-difluorophenyl)-2-propenoate

https://huagongshe.com/reaction/603321

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant(-)-MentholHCID 16666—
Reactant(2E)-3-(3,4-Difluorophenyl)-2-propenoyl chlorideHCID 9920680—
SolventTolueneHCID 1140—
Product(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl (E)-3-(3,4-difluorophenyl)-2-propenoateHCID 10268077—

Reaction Conditions

Temperature65 °C

Reaction Steps

A solution of L-menthol (7.1 kg) in toluene (8.5 kg) was added over a 20 minute period to the solution of (E)-3-(3,4-difluorophenyl)-2-propenoyl chloride (prepared as in Example 2) and pyridine (0.18 kg, 2.28 mol) stirring at 65° C. The reaction mixture was stirred at 65° C. for a further 4 hours and 40 minutes after the addition was complete, then cooled to 25° C. and stirred for a 14 hours. The solution was diluted with toluene (16 kg), washed with 5% aqueous sodium chloride (6.4 kg), then 6% sodium hydrogen carbonate (6.47 kg), then water (6.1 kg). The solution was dried azeotropically by distillation of the solvent (20 L) under reduced pressure. Dimethyl sulfoxide (33.9 kg) was added and the remaining toluene was distilled off under reduced pressure, affording 47.3 kg of a solution of (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl (E)-3-(3,4-difluorophenyl)-2-propenoate (approx. 13.3 kg) in dimethyl sulfoxide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906662B2
Source datasetuspto-grants-2011_03
ORD IDord-f3ed92af4ca241c9bdff8f9a99b60c3f
Source noteuspto-grants-2011_03