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HRID 126862作成日:2026年10月27日

Hydrochloric Acid → 1-(3-Methylphenyl)-2-[1-(phenylmethyl)-4-piperidinyl]ethanone hydrochloride

https://huagongshe.com/reaction/126862

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物IsopropanolHCID 3776—
反応物3-BromotolueneHCID 11560—
反応物Ammonium ChlorideHCID 25517—
反応物1-Benzylpiperidine-4-acetonitrileHCID 562499—
反応物MagnesiumHCID 5462224—
溶媒Diethyl EtherHCID 3283—
生成物1-(3-Methylphenyl)-2-[1-(phenylmethyl)-4-piperidinyl]ethanone hydrochlorideHCID 2028804671%

反応手順

To a stirred and refluxing Grignard-complex, previously prepared starting from 3.65 parts of magnesium, 26 parts of 1-bromo-3-methylbenzene and 70 parts of 1,1'-oxybisethane, is added dropwise a solution of 21.4 parts of 1-(phenylmethyl)-4-piperidineacetonitrile in 70 parts of 1,1'-oxybisethane. Upon completion, stirring is continued for 4 hours at reflux temperature. The reaction mixture is cooled in and ice-bath and decomposed by the addition of a saturated ammonium chloride solution. The layers are separated and the aqueous phase is extracted twice with 1,1'-oxybisethane. The combined organic phases are dried, filtered and evaporated. The oily 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. The oily residue is stirred in 2,2'-oxybispropane with activated charcoal. The latter is filtered off till a clear filtrate is obtained. The filtrate is acidified with 2 -propanol saturated with hydrogen chloride. The whole is evaporated and the residue is crystallized from warm 4-methyl-2-pentanone, yielding 24.5 parts (71%) of 1-(3-methylphenyl)-2-[1-(phenylmethyl)-4-piperidinyl]ethanone hydrochloride; mp. 165.8° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04254127
出典データセットuspto-grants-1981_03
ORD IDord-36ef77958bac493c8045e8d554f0948c
出典メモuspto-grants-1981_03