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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248850Generated: October 27, 2026

Acetic Acid → 2-((1R,3R,4S)-1-methyl-4-isopropylcyclohex-3-yloxy)propionitrile

https://huagongshe.com/reaction/248850

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAcrylonitrileHCID 7855—
Reactant(-)-MentholHCID 16666—
ReactantSodium hydrideHCID 24758—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product2-((1R,3R,4S)-1-methyl-4-isopropylcyclohex-3-yloxy)propionitrileHCID 57204740—

Reaction Steps

1 g of a sodium hydride suspension (50% strength) in paraffin oil was added at a temperature of 0° C. to a solution of 30 g of L-menthol in 300 ml of dichloromethane. A solution of 12.5 ml acrylonitrile in 50 ml dichloromethane was slowly added dropwise, and the reaction mixture was then stirred at room temperature for a further 5 hours. The reaction mixture was worked up by cautiously adding 10 ml of glacial acetic acid, followed by 200 ml of water, and then extracting the mixture with dichloromethane. The dichloromethane extract was dried over sodium sulfate, filtered and concentrated. After chromatographic purification of the residue on silica gel using n-hexane/dichloromethane as the eluent, 25.03 g of crude 2-((1R,3R,4S)-1-methyl-4-isopropylcyclohex-3-yloxy)propionitrile were obtained and used for the next reaction step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05212173
Source datasetuspto-grants-1993_05
ORD IDord-339e1ff250f641c3b64602c0196a7803
Source noteuspto-grants-1993_05