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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 340950생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/340950

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

(S)-5-amino-2-(benzyloxycarbonylamino)pentanoic acid (10.0 g, 37.56 mmol) and ethyl 1,3-dioxoisoindoline-2-carboxylate (9.04 g, 41.28 mmol) in NMP (40.0 mL) were heated to 150° C. for 30 min in 4 microwave reaction tubes. The mixture was diluted with EtOAc (500 mL). The organic mixture was washed with water (100 mL×2) and brine, dried over Na2SO4, filtered, and concentrated under reduced pressure to give an oil, which was redissolved in toluene. To the resulting solution were added paraformaldehyde, PTSA and molecular sieves (3 A) and the mixture was heated to 150° C. for 20 min in a microwave reactor. The reaction mixture was diluted with ether (800 mL), washed with NaHCO3 and brine, dried over Na2SO4, filtered, and concentrated under reduced pressure. The residue was purified on silica gel 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 번호US08895582B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-7b98d7b8016e43bab56041ff2c72cb2e
출처 메모uspto-grants-2014_11