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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 261491생성일: 2026년 10월 26일

1-Benzyl-4-piperidone → 1-Benzyl-4-(4-chloro-2-fluorobenzyl)-4-piperidinol

https://huagongshe.com/reaction/261491

반응식

참여 물질

역할이름HCID투입량
반응물1-Benzyl-4-piperidoneHCID 19220—
반응물4-Chloro-2-fluorobenzyl bromideHCID 2736551—
생성물1-Benzyl-4-(4-chloro-2-fluorobenzyl)-4-piperidinolHCID 12733222—

반응 단계

A sample of 4-chloro-2-fluorobenzyl bromide is converted to its Grignard reagent which is reacted with N-benzyl-4-piperidone to provide 1-benzyl-4-(4-chloro-2-fluorobenzyl)-4-piperidinol in the manner described in Example 4A. This product is distilled at 175°-180° C., 0.18 mm, to provide an orange oil which is converted in ether to its hydrogen chloride salt. The salt is recrystallized four times from an ethyl alcohol-ether mixture to provide the purified salt, mp 211.5°-213° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04166119
출처 데이터셋uspto-grants-1979_08
ORD IDord-8bf40db80661482e915220dfee4b2b9e
출처 메모uspto-grants-1979_08