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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1156031생성일: 2026년 10월 27일

Ethyl chloroformate → 1-Ethoxycarbonyl-4-phenoxy-4-phenylpiperidine

https://huagongshe.com/reaction/1156031

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl chloroformateHCID 10928—
반응물Piperidine, 1-methyl-4-phenoxy-4-phenyl-HCID 3060394—
생성물1-Ethoxycarbonyl-4-phenoxy-4-phenylpiperidineHCID 20536603—

반응 단계

9.0 g of 1-methyl-4-phenoxy-4-phenylpiperidine are added in portions of 100 ml of chloroformic acid ethyl ester at 80° C.; severe foaming is observed during this addition. When the addition has ended, the mixture is boiled under reflux for 3 hours, excess chloroformic acid ethyl ester is distilled off in vacuo, and 120 ml of water and 15 ml of concentrated ammonia are added to resulting solid residue. This mixture is stirred thoroughly, and the precipitate is filtered off and rinsed with water. The 1-ethoxycarbonyl-4-phenoxy-4-phenylpiperidine (m.p. 117° to 118° C., from ethanol) thus obtained is boiled under reflux with a solution of 15 g of potassium hydroxide in 150 ml of n-butanol for 4 hours; after cooling, 300 ml of water are added to the solution, and the obtained mixture is extracted twice with diethyl ether. The combined organic phases are dried over sodium sulfate and concentrated. The title compound remains as a brownish oil. The hydrochloride melts at 192° C. (from ethanol).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04333942
출처 데이터셋uspto-grants-1982_06
ORD IDord-30cf66b11ed94c99813e5bb7aab0b6b6
출처 메모uspto-grants-1982_06