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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

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물1-[3-(6-Fluoro-1,2-benzisoxazol-3-yl)propyl]-4-piperidoneHCID 13207819—
반응물HCID 178418276HCID 178418276—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물1-[3-(6-Fluoro-1,2-benzisoxazol-3-yl)propyl]-4-hydroxy-4-(4-methoxyphenyl)piperidine hydrochlorideHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04396770
출처 데이터셋uspto-grants-1983_08
ORD IDord-c19ce0116b8849bba4849a32a844be42
출처 메모uspto-grants-1983_08