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HRID 269883作成日:2026年10月24日

Phenacyl bromide → HCID 23111474、化合物

https://huagongshe.com/ja/reaction/269883

反応式

関与物質

役割名称HCID仕込み量
反応物Phenacyl bromideHCID 6259—
反応物Phenethyl bromideHCID 7666—
反応物1-(4-Methoxyphenyl)-piperazine, dihydrochlorideHCID 2723700—
反応物1-(3-Chloro-4-methoxymethoxyphenyl)-piperazineHCID 23111401—
生成物HCID 23111474HCID 2311147416.7%

反応手順

Production Example 1 was repeated except that 1-(4-methoxyphenyl)piperazine dihydrochloride and (2-bromoethyl)-benzene were replaced with 1-(3-chloro-4-methoxymethoxyphenyl)-piperazine (924 mg) and 2-bromoacetophenone (789 mg), respectively. Thus obtained crude product was purified on silica gel column chromatography (eluent, chloroform: acetone=20:1), to provide 2-[4-(3-chloro-4-methoxymethoxyphenyl)piperazin-1-yl]-1-phenylethan-1-one (225 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07449466B2
出典データセットuspto-grants-2008_11
ORD IDord-9285a092300e433b9772f00c2f935372
出典メモuspto-grants-2008_11