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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196264Generated: October 31, 2026

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → 4,4-Diphenyl-2-formyl-2-cyclohexen-1-one

https://huagongshe.com/reaction/1196264

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
ReactantHCID 54244847HCID 54244847—
Solvent1,4-DioxaneHCID 31275—
Product4,4-Diphenyl-2-formyl-2-cyclohexen-1-oneHCID 5379475327.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 4,4-diphenyl-2-formylcyclohexanone (44.5 g) and 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (38 g) in dioxane (650 cc) is stirred for 30 minutes at 25° C. and then cooled to 0° C.; the solid is removed by filtration and the filtrate is concentrated to dryness under reduced pressure (2.7 kPa). The residue is chromatographed on a column of silica gel (0.2-0.06 mm, diameter 6 cm, height 63 cm), eluting with a mixture of cyclohexane and ethyl acetate (80:20 by volume) and collecting 50-cc fractions. Fractions 7 to 12 are combined and concentrated to dryness under reduced pressure (2.7 kPa). The crystalline residue is stirred vigorously with isopropyl ether (200 cc) and the crystals obtained are drained, washed with isopropyl ether (2×50 cc) and dried. 4,4-Diphenyl-2-formyl-2-cyclohexen-1-one (12 g), m.p. 126° C., is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05112988
Source datasetuspto-grants-1992_05
ORD IDord-f2d4818838cf492a912d31a4e29e5f05
Source noteuspto-grants-1992_05