Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 28151생성일: 2026년 10월 25일
Triethylamine → N-(4-chlorophenyl)-N-(1-propyl-4-piperidinyl)benzeneacetamide hydrochloride
https://huagongshe.com/reaction/28151
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 1-Iodopropane | HCID 33643 | — |
| 반응물 | N-(4-Chlorophenyl)-N-4-piperidinylbenzeneacetamide | HCID 162188 | — |
| 용매 | Benzene | HCID 241 | — |
| 생성물 | N-(4-chlorophenyl)-N-(1-propyl-4-piperidinyl)benzeneacetamide hydrochloride | HCID 23339041 | — |
반응 단계
To a stirred solution of 4 parts of N-(4-chlorophenyl)-N-(4-piperidinyl)benzeneacetamide and 3 parts of N,N-diethylethanamine in 200 parts of benzene are added portionwise 4 parts of 1-iodopropane and the whole is stirred and refluxed for 47 hours. Then the second portion of 4 parts of 1-iodopropane is added and stirring and refluxing is continued for another 20 h.20. The reaction mixture is cooled and filtered. The filtrate is washed with water, dried and evaporated in vacuo. From the oily free base, the hydrochloride salt is prepared in the conventional manner in 1,1'-oxybisethane. The precipitated solid salt is filtered off and dried, yielding 3.5 parts of N-(4-chlorophenyl)-N-(1-propyl-4-piperidinyl)benzeneacetamide hydrochloride; mp. 233.5° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04225606 |
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| 출처 데이터셋 | uspto-grants-1980_09 |
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| ORD ID | ord-e2192b2ec0f648c4994e1497b6c9c192 |
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| 출처 메모 | uspto-grants-1980_09 |
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