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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 538921생성일: 2026년 10월 24일

4-Methylmorpholine → Phenylmethyl (3S)-3-[[(1,1-dimethylethoxy)carbonyl]amino]-4-hydroxybutanoate

https://huagongshe.com/ko/reaction/538921

반응식

참여 물질

역할이름HCID투입량
반응물4-MethylmorpholineHCID 7972—
반응물Isobutyl chloroformateHCID 62365—
반응물N-tert-Butoxycarbonyl-L-aspartic acid beta-benzyl esterHCID 1581888—
반응물Sodium borohydrideHCID 4311764—
용매1,2-DimethoxyethaneHCID 8071—
생성물Phenylmethyl (3S)-3-[[(1,1-dimethylethoxy)carbonyl]amino]-4-hydroxybutanoateHCID 10040985—

반응 조건

온도-20 °C

반응 단계

To a solution of Boc-L-aspartic acid-4-benzyl ester (100 g, 309 mmol) in DME (1.8 L) at −20° C. was added NMM (34 mL, 309 mmol) then dropwise iso-butylchloroformate (40 mL, 309 mmol) and the mixture was stirred at −20° C. for 20 min. The reaction mixture was filtered and the filtrate was cooled to −20° C. NaBH4 (17.5 g, 463 mmol) was added portionwise at −20° C. The mixture was allowed to warm and stirred at rt for 1 h. The mixture was quenched with a 20% citric acid solution and then extracted with AcOEt. The organic layer was washed with NaHCO3 solution, H2O and brine, dried (MgSO4), filtered and concentrated. The product was used without further purification for the next step.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08865894B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-379a98ce8165465aad03657a829ab132
출처 메모uspto-grants-2014_10