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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1380243생성일: 2026년 10월 25일

Ammonium Chloride → alpha-(4-Fluorophenyl)-alpha-(1-methyl-4-piperidinyl)-3-pyridinemethanol

https://huagongshe.com/reaction/1380243

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물4-chloro-N-methylpiperidineHCID 79342—
반응물(4-Fluorophenyl)(pyridin-3-yl)methanoneHCID 762660—
반응물MagnesiumHCID 5462224—
용매TolueneHCID 1140—
용매TetrahydrofuranHCID 8028—
생성물alpha-(4-Fluorophenyl)-alpha-(1-methyl-4-piperidinyl)-3-pyridinemethanolHCID 2332605495%

반응 단계

To a stirred and cooled Grignard-complex previously prepared starting from a mixture of 134 parts of 4-chloro-1-methylpiperidine, 25 parts of magnesium and 652.5 parts of tetrahydrofuran was added dropwise a solution of 170 parts of (4-fluorophenyl)(3-pyridinyl)methanone in 405 parts of tetrahydrofuran at a temperature between 10°-20° C. Upon completion, stirring was continued for 1 hour at room temperature and for 30 minutes at minutes at reflux. After cooling, the whole was decomposed by pouring onto a mixture of crushed ice and ammonium chloride. 270 Parts of methylbenzene were added. The organic layer was separated, dried, filtered and evaporated. The residue was boiled in acetonitrile with activated charcoal. The latter was filtered off over Hyflo and the filtrate was evaporated, yielding 240 parts (95%) of α-(4-fluorophenyl)-α-(1-methyl-4-piperidinyl)-3-pyridinemethanol as a residue (intermediate 18).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04581171
출처 데이터셋uspto-grants-1986_04
ORD IDord-6c0e3012146947ae9a6e5ab2b7efde83
출처 메모uspto-grants-1986_04