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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358293Generated: October 29, 2026

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → HCID 12877518, compound

https://huagongshe.com/reaction/358293

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
Reactant1,4-DioxaneHCID 31275—
ReactantHCID 12877516HCID 12877516—
SolventEthyl acetate hexaneHCID 21226206—
ProductHCID 12877518HCID 1287751891.3%

Reaction Steps

Into 6 ml of dioxane, were dissolved 500 mg of 4-hydroxy-5-allyl-2-cyclopentenone and 450mg of 2,3-dichloro-5,6-dicyano-1,4-benzoquinone. The solution was left standing at room temperature for 16 hours and the precipitated 2,3-dichloro-5,6-dicyanohydroquinone was collected by filtration and washed with methylene chloride. The filtrate together with the washings was concentrated. The concentration residue was dissolved in 50 ml of methylene chloride, washed with a 10% aqueous sodium hydroxide solution, then with water until the washings had become neutral. The residue thus treated was dried over anhydrous sodium sulfate, stripped of the solvent by distillation, and purified by column chromatography using 20 g of a silica gel (Wako Gel C-200) and an ethyl acetate-n-hexane (2:3 by volume) mixture as eluent, to obtain 450 mg (91% yield) of 4-keto-5-allyl-2-cyclopentenone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04465862
Source datasetuspto-grants-1984_08
ORD IDord-f117e63554cb4e0db722668f2035f077
Source noteuspto-grants-1984_08