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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 848135생성일: 2026년 10월 26일

Thionyl Chloride → Benzyl-rac-{1-[[2-(o-fluorobenzoyl)-4-nitrophenyl]carbamoyl]butyl}carbamate

https://huagongshe.com/reaction/848135

반응식

참여 물질

역할이름HCID투입량
반응물Thionyl ChlorideHCID 24386—
반응물2-Amino-2'-fluoro-5-nitrobenzophenoneHCID 67657—
반응물N-[(Benzyloxy)carbonyl]norleucineHCID 263476—
용매TetrahydrofuranHCID 8028—
생성물Benzyl-rac-{1-[[2-(o-fluorobenzoyl)-4-nitrophenyl]carbamoyl]butyl}carbamateHCID 131712305—

반응 단계

19.7 g of N-carbobenzoxy-DL-norleucine are dissolved in 200 ml of absolute tetrahydrofuran, the solution is treated dropwise while cooling with ice with 10 g of thionyl chloride and then stirred for 1 hour. To this solution there is rapidly added dropwise a solution of 17 g (0.065 M) of 2-amino-5-nitro-2'-fluorobenzophenone in 130 ml of absolute tetrahydrofuran and the mixture is then stirred at room temperature for 60 hours. The solution is concentrated and the residue is treated with ice and 10% sodium bicarbonate solution and extracted with methylene chloride. The organic solution is dried with sodium sulphate, filtered and concentrated. The residue is purified on a 450 g silica gel column using methylene chloride as the eluting agent and crystallised from ethanol. There is obtained benzyl-rac-{1-[[2-(o-fluorobenzoyl)-4-nitrophenyl]carbamoyl]butyl}carbamate which melts at 148°-150° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04294758
출처 데이터셋uspto-grants-1981_10
ORD IDord-cc1e2d0aad534da1b8c06678a426964d
출처 메모uspto-grants-1981_10