Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 434406생성일: 2026년 10월 26일
Ammonium Chloride → 1-[3-(6-Fluoro-1,2-benzisoxazol-3-yl)propyl]-4-hydroxy-4-(4-methoxyphenyl)piperidine hydrochloride
https://huagongshe.com/reaction/434406
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | 1-[3-(6-Fluoro-1,2-benzisoxazol-3-yl)propyl]-4-piperidone | HCID 13207819 | — |
| 반응물 | HCID 178418276 | HCID 178418276 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1-[3-(6-Fluoro-1,2-benzisoxazol-3-yl)propyl]-4-hydroxy-4-(4-methoxyphenyl)piperidine hydrochloride | HCID 13207827 | — |
반응 단계
A solution of 6.3 g of 1-[3-(6-fluoro-1,2-benzisoxazol-3-yl)propyl]-4-piperidone in 35 ml of tetrahydrofuran was slowly added to a solution of 49 ml of p-anisylmagnesium bromide (1.4 M in tetrahydrofuran). After the addition was complete, the reaction mixture was stirred at ambient temperature for one hr, diluted with ether, poured into 400 of ml saturated ammonium chloride solution and extracted with ether. The organic extracts were washed with water (2×), saturated sodium chloride solution and dried over anhydrous magnesium sulfate, filtered and concentrated. The residue was converted to 8.5 g (89%) of product, mp 100°-105° C., by treatment with ethereal hydrogen chloride. An analytical sample was obtained by recrystallization from ethyl acetate/methanol and had mp 181°-182° C. (dec).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04396770 |
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| 출처 데이터셋 | uspto-grants-1983_08 |
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| ORD ID | ord-c19ce0116b8849bba4849a32a844be42 |
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| 출처 메모 | uspto-grants-1983_08 |
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