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HRID 486437作成日:2026年10月26日

1-Bromo-3-chlorobenzene → 3-(3-Chlorophenyl)-1-(phenylmethyl)-3-piperidinol hydrochloride

https://huagongshe.com/reaction/486437

反応式

関与物質

役割名称HCID仕込み量
反応物1-Bromo-3-chlorobenzeneHCID 7928—
反応物TetrahydrofuranHCID 8028—
反応物3-Piperidinone, 1-(phenylmethyl)-HCID 96650—
反応物MagnesiumHCID 5462224—
溶媒Acetic AcidHCID 176—
生成物3-(3-Chlorophenyl)-1-(phenylmethyl)-3-piperidinol hydrochlorideHCID 1909558676%

反応手順

To a stirred and refluxed Grignard complex previously prepared starting from a mixture of 4.2 parts of 1-bromo-3-chlorobenzene, 5.4 parts of magnesium and 135 parts of tetrahydrofuran were added dropwise 19 parts of 1-(phenylmethyl)-3-piperidinone. Upon completion, stirring was continued for 1 hour at reflux temperature. After cooling, the reaction mixture was poured into ice water and 12.5 parts of acetic acid. The layers were separated. The aqueous phase was extracted with trichloromethane. The organic layer was washed with water, dried, filtered and evaporated. The residue was converted into the hydrochloride salt in 2-propanol. The salt was filtered off and dried, yielding 26 parts (76%) of 3-(3-chlorophenyl)-1-(phenylmethyl)-3-piperidinol hydrochloride (intermediate 27).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05292738
出典データセットuspto-grants-1994_03
ORD IDord-6aaafb2e7202497f9a681d221835f2e6
出典メモuspto-grants-1994_03