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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 848522생성일: 2026년 10월 24일

Thionyl Chloride → Rac-benzyl-{1-[[2-(o-fluorobenzoyl)-4-nitrophenyl]carbamoyl]ethyl}carbamate

https://huagongshe.com/ko/reaction/848522

반응식

참여 물질

역할이름HCID투입량
반응물Thionyl ChlorideHCID 24386—
반응물2-Amino-2'-fluoro-5-nitrobenzophenoneHCID 67657—
반응물N-(Benzyloxycarbonyl)-DL-alanineHCID 95657—
용매TetrahydrofuranHCID 8028—
생성물Rac-benzyl-{1-[[2-(o-fluorobenzoyl)-4-nitrophenyl]carbamoyl]ethyl}carbamateHCID 20562333—

반응 단계

50 g of carbobenzoxy-DL-alanine are dissolved in 400 ml of absolute tetrahydrofuran, treated dropwise while cooling with ice with 30 g of thionyl chloride and stirred for 40 minutes, a suspension of 50 g of 2-amino-5-nitro-2'-fluorobenzophenone in 200 ml of absolute tetrahydrofuran then being rapidly added dropwise. Subsequently, the mixture is stirred at room temperature for 18 hours, the solution is concentrated and the residue is treated with ice and 10% sodium bicarbonate solution. The mixture is extracted with methylene chloride, the organic solution is dried with sodium sulphate, filtered and concentrated. The residue is crystallised from ethanol and yields rac-benzyl-{1-[[2-(o-fluorobenzoyl)-4-nitrophenyl]carbamoyl]ethyl}carbamate which is further processed directly as the crude product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04296031
출처 데이터셋uspto-grants-1981_10
ORD IDord-d7a69e9e3dc244e2a5f268bf7949bb71
출처 메모uspto-grants-1981_10