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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 483313생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물2-Chloro-1,4-naphthoquinoneHCID 13891—
반응물Ammonium PersulfateHCID 62648—
반응물4-(4-Chlorophenyl)cyclohexane-1-carboxylic acidHCID 2735792—
촉매Silver NitrateHCID 24470—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
생성물1,4-Naphthalenedione, 2-chloro-3-[cis-4-(4-chlorophenyl)cyclohexyl]-HCID 1110107035%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05225184
출처 데이터셋uspto-grants-1993_07
ORD IDord-37f13d8a79d8464e8955a3260e3cf361
출처 메모uspto-grants-1993_07