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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 893829생성일: 2026년 10월 25일

Ethyl chloroformate → 4-(2,3,4-Trimethoxybenzylthio)-1-cinnamylpiperidine

https://huagongshe.com/reaction/893829

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl chloroformateHCID 10928—
반응물Potassium HydroxideHCID 14797—
반응물Toluene, alpha-chloro-2,3,4-trimethoxy-HCID 97491—
반응물SodiumHCID 5360545—
반응물FumarateHCID 5460307—
반응물1-Methylpiperidine-4-thiolHCID 14180391—
반응물4-(2,3,4-Trimethoxybenzylthio)-1-ethoxycarbonylpiperidineHCID 19890907—
반응물4-(2,3,4-Trimethoxybenzylthio)-1-cinnamylpiperidine fumarateHCID 67894540—
용매BenzeneHCID 241—
용매EthanolHCID 702—
생성물4-(2,3,4-Trimethoxybenzylthio)-1-cinnamylpiperidineHCID 53752093—

반응 단계

The 4-(2,3,4-trimethoxybenzylthio)piperidine used as starting material, the fumarate of which melts at 154° C., was prepared by the hydrolysis, using potassium hydroxide and ethanol, of 4-(2,3,4-trimethoxybenzylthio)-1-ethoxycarbonylpiperidine (oil), which was itself prepared by the action of ClCOOC2H5 in benzene on 4-(2,3,4-trimethoxybenzylthio)-1-methylpiperidine (m.p. of the corresponding fumarate: 130° C.), which was itself prepared by the condensation of 2,3,4-trimethoxybenzyl chloride in ethanol with the sodium salt of 1-methyl-4-mercaptopiperidine, b.p./13 : 70°-72° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05126356
출처 데이터셋uspto-grants-1992_06
ORD IDord-723d3b8048ee46d3b6b86ab349d9e5a4
출처 메모uspto-grants-1992_06