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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 248850생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/248850

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물AcrylonitrileHCID 7855—
반응물(-)-MentholHCID 16666—
반응물Sodium hydrideHCID 24758—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물2-((1R,3R,4S)-1-methyl-4-isopropylcyclohex-3-yloxy)propionitrileHCID 57204740—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05212173
출처 데이터셋uspto-grants-1993_05
ORD IDord-339e1ff250f641c3b64602c0196a7803
출처 메모uspto-grants-1993_05