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HRID 483313作成日:2026年10月23日

2-Chloro-1,4-naphthoquinone → 1,4-Naphthalenedione, 2-chloro-3-[cis-4-(4-chlorophenyl)cyclohexyl]-

https://huagongshe.com/ja/reaction/483313

反応式

関与物質

役割名称HCID仕込み量
反応物2-Chloro-1,4-naphthoquinoneHCID 13891—
反応物Ammonium PersulfateHCID 62648—
反応物4-(4-Chlorophenyl)cyclohexane-1-carboxylic acidHCID 2735792—
触媒Silver NitrateHCID 24470—
溶媒WaterHCID 962—
溶媒AcetonitrileHCID 6342—
生成物1,4-Naphthalenedione, 2-chloro-3-[cis-4-(4-chlorophenyl)cyclohexyl]-HCID 1110107035%

反応手順

A mixture of 2-chloro-1,4-naphthoquinone (3.95 g, 0.02 mol), 4-(4-chlorophenyl)cyclohexane-1-carboxylic acid (4.9 g, 0.02 mol) and powdered silver nitrate (1.05 g, 0.0062 mol) was heated to reflux with vigorous stirring in 40 ml of acetonitrile. A solution of ammonium persulphate (12.0 g, 0.0525 mol) in 50 ml of water was added dropwise over 1 hour. The mixture was refluxed for 3 hours the cooled in ice for 30 mins, after which it was filtered, and the residual sticky solid extracted twice with boiling chloroform to remove inorganic material. The chloroform was removed by evaporation to leave a yellow-brown solid (ca 2.7 g). This was dissolved in 40 ml of boiling acetonitrile; a little insoluble material was removed by filtration. On cooling, the title compound separated as yellow crystals, (550 mg) m.p. 172°-175° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05225184
出典データセットuspto-grants-1993_07
ORD IDord-37f13d8a79d8464e8955a3260e3cf361
出典メモuspto-grants-1993_07