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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703143Generated: October 26, 2026

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

https://huagongshe.com/reaction/703143

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-1,4-naphthoquinoneHCID 13891—
ReactantAmmonium PersulfateHCID 62648—
Reactant4-(4-Chlorophenyl)cyclohexane-1-carboxylic acidHCID 2735792—
CatalystSilver NitrateHCID 24470—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product1,4-Naphthalenedione, 2-chloro-3-[cis-4-(4-chlorophenyl)cyclohexyl]-HCID 1110107035%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04981874
Source datasetuspto-grants-1991_01
ORD IDord-19c70a89ebce40fb8dafee85e0c5c210
Source noteuspto-grants-1991_01