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HRID 1380243作成日:2026年10月26日

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

https://huagongshe.com/reaction/1380243

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物4-chloro-N-methylpiperidineHCID 79342—
反応物(4-Fluorophenyl)(pyridin-3-yl)methanoneHCID 762660—
反応物MagnesiumHCID 5462224—
溶媒TolueneHCID 1140—
溶媒TetrahydrofuranHCID 8028—
生成物alpha-(4-Fluorophenyl)-alpha-(1-methyl-4-piperidinyl)-3-pyridinemethanolHCID 2332605495%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04581171
出典データセットuspto-grants-1986_04
ORD IDord-6c0e3012146947ae9a6e5ab2b7efde83
出典メモuspto-grants-1986_04