돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 416348생성일: 2026년 10월 24일

Formaldehyde → (S)-benzyl 4-(3-(1,3-dioxoisoindolin-2-yl)propyl)-5-oxooxazolidine-3-carboxylate

https://huagongshe.com/ko/reaction/416348

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물p-Toluenesulfonic acidHCID 6101—
반응물N-CarbethoxyphthalimideHCID 31187—
반응물N-alpha-Benzyloxycarbonyl-L-ornithineHCID 7010490—
용매TolueneHCID 1140—
용매Diethyl EtherHCID 3283—
용매Ethyl AcetateHCID 8857—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물(S)-benzyl 4-(3-(1,3-dioxoisoindolin-2-yl)propyl)-5-oxooxazolidine-3-carboxylateHCID 5438015676%

반응 조건

온도150 °C

반응 단계

A mixture of (S)-5-amino-2-(benzyloxycarbonylamino)pentanoic acid (10.0 g, 37.56 mmol), ethyl 1,3-dioxoisoindoline-2-carboxylate (9.04 g, 41.28 mmol) in NMP (40.0 mL) was heated to 150° C. for 30 min in 4 microwave reaction tubes. The mixture was diluted with EtOAc (500 mL). The organic layer washed with water (100 mL×2), brine, dried over Na2SO4, filtered, and concentrated under reduced pressure to give an oil, which was dissolved in toluene. To this toluene solution was added paraformaldehyde, PTSA and molecular sieves (3 Å) and the mixture was heated to 150° C. for 20 min. The mixture was diluted with ether (800 mL), washed with NaHCO3, brine, dried over Na2SO4, filtered, and concentrated under reduced pressure. The crude was purified on silica gel column using a mixture of EtOAc and hexanes to give (S)-benzyl 4-(3-(1,3-dioxoisoindolin-2-yl)propyl)-5-oxooxazolidine-3-carboxylate (11.6 g, 76% for 2 steps).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08088793B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-72832e885ee74b96ab642b978891e8de
출처 메모uspto-grants-2012_01