Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
1-Benzyl-4-piperidone → 1-Benzyl-4-(4-chloro-2-fluorobenzyl)-4-piperidinol
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 1-Benzyl-4-piperidone | HCID 19220 | — |
| 반응물 | 4-Chloro-2-fluorobenzyl bromide | HCID 2736551 | — |
| 생성물 | 1-Benzyl-4-(4-chloro-2-fluorobenzyl)-4-piperidinol | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04166119 |
| 출처 데이터셋 | uspto-grants-1979_08 |
| ORD ID | ord-8bf40db80661482e915220dfee4b2b9e |
| 출처 메모 | uspto-grants-1979_08 |