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HRID 1028851생성일: 2026년 10월 27일

2,6-Di-tert-butyl-4-methylpyridine → (S)-3-tert-Butoxycarbonylamino-4-methoxy-butyric acid benzyl ester

https://huagongshe.com/reaction/1028851

반응식

참여 물질

역할이름HCID투입량
반응물2,6-Di-tert-butyl-4-methylpyridineHCID 98898—
반응물Oxonium, trimethyl-, tetrafluoroborate(1-) (1:1)HCID 2735153—
반응물Phenylmethyl (3S)-3-[[(1,1-dimethylethoxy)carbonyl]amino]-4-hydroxybutanoateHCID 10040985—
용매DichloromethaneHCID 6344—
생성물(S)-3-tert-Butoxycarbonylamino-4-methoxy-butyric acid benzyl esterHCID 57976545—

반응 단계

To tert-butyl (S)-1-((benzyloxy)carbonyl)-3-hydroxypropan-2-ylcarbamate (1 eq.) in dichloromethane was added 2,6-di-t-butyl 4-methylpyridine (2.5 eq.) and trimethyloxonium tetrafluoroborate (1.25 eq.) at 0° C. The reaction mixture was gradually warm to room temperature and stirred overnight. The reaction mixture was diluted with dichloromethane and washed with cold satd. sodium bicarbonate, water, and brine and dried over sodium sulfate. Purification by silica gel chromatography (25% EtOAc/Hexane) provide pure product as a colorless viscous liquid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08735599B2
출처 데이터셋uspto-grants-2014_05
ORD IDord-25f5154284424362bfc7d37f46dc4d04
출처 메모uspto-grants-2014_05