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HRID 66675作成日:2026年10月24日

Water → (4-Bromophenyl)-(1-methyl-4-piperidinyl)methanone

https://huagongshe.com/ja/reaction/66675

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Benzonitrile, 4-bromo-HCID 12162—
反応物Ammonium ChlorideHCID 25517—
反応物4-chloro-N-methylpiperidineHCID 79342—
反応物MagnesiumHCID 5462224—
溶媒TetrahydrofuranHCID 8028—
生成物(4-Bromophenyl)-(1-methyl-4-piperidinyl)methanoneHCID 20530733—

反応手順

To a stirred and cooled (10°-15° C.) Grignard-complex, previously prepared starting from 13.5 parts of 4-chloro-1-methylpiperidine and 2.4 parts of magnesium in 68 parts of tetrahydrofuran, is added dropwise a solution of 10 parts of 4-bromobenzonitrile in 22 parts of tetrahydrofuran. Upon completion, stirring is continued for 1 hour at reflux temperature. The reaction mixture is decomposed by pouring onto a mixture of 50 parts of ammonium chloride in 250 parts of water. The product is extracted with methylbenzene. The extract is dried, filtered and evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions are collected and the eluent is evaporated, yielding 10 parts of (4-bromophenyl)-(1-methyl-4-piperidinyl)methanone as a residue.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04342870
出典データセットuspto-grants-1982_08
ORD IDord-93eec3e9667745f9b5688539be76b279
出典メモuspto-grants-1982_08