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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone | HCID 6775 | — |
| Reactant | HCID 54244847 | HCID 54244847 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4,4-Diphenyl-2-formyl-2-cyclohexen-1-one | HCID 53794753 | 27.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05112988 |
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| Source dataset | uspto-grants-1992_05 |
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| ORD ID | ord-f2d4818838cf492a912d31a4e29e5f05 |
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| Source note | uspto-grants-1992_05 |
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