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HRID 484733作成日:2026年10月26日

Ammonium Chloride → alpha-(2-Fluorophenyl)-1-methyl-alpha-phenyl-4-piperidinemethanol

https://huagongshe.com/reaction/484733

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2-FluorobenzophenoneHCID 67650—
反応物4-chloro-N-methylpiperidineHCID 79342—
反応物MagnesiumHCID 5462224—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物alpha-(2-Fluorophenyl)-1-methyl-alpha-phenyl-4-piperidinemethanolHCID 2332606544%

反応条件

温度0 °C

反応手順

To a stirred and refluxing Grignard complex previously prepared starting from 80.2 parts of 4-chloro-1-methylpiperidine, 14.6 parts of magnesium and 270 parts of tetrahydrofuran, was added dropwise a solution of 101 parts of (2-fluorophenyl)phenylmethanone in 450 parts of tetrahydrofuran. Upon completion, stirring was continued for 18 hours at reflux temperature. The reaction mixture was cooled in an ice-bath and decomposed with a solution of 32 parts of ammonium chloride in 160 parts of water. After stirring for 30 minutes, the product was filtered off and washed with tetrahydrofuran. The filtrate was evaporated, the residue was taken up in methylbenzene and the latter was evaporated again in a boiling water-bath. The residue was dissolved in 700 parts of 2,2'-oxybispropane. The turbid solution was filtered and gaseous hydrogen chloride was bubbled through the filtrate. The solid product was filtered off and suspended in 1000 parts of water. The suspension was treated with ammonium hydroxide and extracted twice with 280 parts of 1,1'-oxybisethane. The combined extracts were dried, filtered and evaporated. The oily residue was crystallized from 240 parts of acetonitrile. After cooling to 0° C., the product was filtered off and dried, yielding 66 parts (44%) of α-(2-fluorophenyl)-1-methyl-α-phenyl-4-piperidinemethanol (intermediate 33).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04533665
出典データセットuspto-grants-1985_08
ORD IDord-9191ce33cb1945b78c98a3f325d17c35
出典メモuspto-grants-1985_08