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HRID 1881340생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1881340

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 번호US08318791B2
출처 데이터셋uspto-grants-2012_11
ORD IDord-ceefe33eeb8544f98d0026339843a731
출처 메모uspto-grants-2012_11