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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 246707생성일: 2026년 10월 24일

Benzyl chloroformate → Ethyl 1-(((benzyloxy)carbonyl)amino)cyclopropanecarboxylate

https://huagongshe.com/ko/reaction/246707

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참여 물질

역할이름HCID투입량
반응물Benzyl chloroformateHCID 10387—
반응물Ethyl 1-aminocyclopropane-1-carboxylate hydrochlorideHCID 386203—
반응물Sodium BicarbonateHCID 516892—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물Ethyl 1-(((benzyloxy)carbonyl)amino)cyclopropanecarboxylateHCID 1313474991%

반응 조건

온도0 °C

반응 단계

A suspension of ethyl 1-aminocyclopropanecarboxylate hydrochloride (9.5 g, 57.3 mmol) in 450 mL of ethyl acetate was cooled to 0° C., a solution of NaHCO3 (39.5 g, 470.3 mmol) in 325 mL of water was added slowly. Then benzyl chloroformate (13.3 g, 78.2 mmol) was added drop-wise. The cold bath was removed and the mixture was stirred at room temperature for 16 hours. The organic phase was washed with 1N HCl (100 mL), saturated NaHCO3 solution (100 mL), brine (100 mL), and dried over anhydrous sodium sulfate. The drying agent was removed by filtration and the filtrate was concentrated to give a white solid. The solid was purified by column chromatography (silica gel, 200-300 mesh, eluting with a mixture of ethyl acetate and petroleum ether (1:3, v/v) to give ethyl 1-(benzyloxycarbonylamino)cyclopropanecarboxylate (13.7 g, 91%) as a white solid. MS: (M+H)+=286.1; 1H NMR (300 MHz, CDCl3): δ 7.37-7.32 (m, 5H), 5.13 (s, 2H), 4.70 (s, 1H), 4.13 (brs, 2H), 1.59-1.53 (m, 2H), 1.23-1.19 (m, 5H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08658646B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-04b0d670ab73489eaffc94edfd1fae0a
출처 메모uspto-grants-2014_02