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HRID 1886565作成日:2026年10月27日

1-Chloro-4-(chloromethyl)benzene → 1-[(4-Chlorophenyl)methyl]-4,4,6-trimethylcyclohex-2-en-1-ol

https://huagongshe.com/reaction/1886565

反応式

関与物質

役割名称HCID仕込み量
反応物1-Chloro-4-(chloromethyl)benzeneHCID 7723—
反応物Ammonium ChlorideHCID 25517—
反応物2-Cyclohexen-1-one, 4,4,6-trimethyl-HCID 114507—
反応物MagnesiumHCID 5462224—
溶媒Diethyl EtherHCID 3283—
生成物1-[(4-Chlorophenyl)methyl]-4,4,6-trimethylcyclohex-2-en-1-olHCID 19771302—

反応手順

To a slurry of magnesium turnings (66 g, 2.73 g atoms) in diethyl ether (300 ml) was added a solution of 4-chlorobenzyl chloride (418 g, 2.6 moles) in diethyl ether (1500 ml) at such a rate as to maintain gentle reflux. After a further 30 minutes, a solution of 4,4,6-trimethylcyclohex-2-en-1-one (340 g, 2.46 moles) in diethyl ether (350 ml) was added, again maintaining a gentle reflux. After 1 hour the mixture was added into saturated aqueous ammonium chloride (4 liters) and the phases separated. The ether phase was back-washed with water (1 liter) and used directly in the next reaction. A small portion of 1-(4-chlorobenzyl)-4,4,6-trimethylcyclohex-2-en-1-ol was isolated for characterisation (gas chromatography analysis showed two isomers in approximately equal amounts).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05151550
出典データセットuspto-grants-1992_09
ORD IDord-09fcd51e7a864ab9b60bd36e94d954ac
出典メモuspto-grants-1992_09