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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone | HCID 6775 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 12877516 | HCID 12877516 | — |
| Solvent | Ethyl acetate hexane | HCID 21226206 | — |
| Product | HCID 12877518 | HCID 12877518 | 91.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04465862 |
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| Source dataset | uspto-grants-1984_08 |
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| ORD ID | ord-f117e63554cb4e0db722668f2035f077 |
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| Source note | uspto-grants-1984_08 |
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