HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2419545Generated: October 25, 2026
2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → 6-Hydroxy-7-methoxy-5-benzofurancarboxaldehyde
https://huagongshe.com/reaction/2419545
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone | HCID 6775 | — |
| Reactant | 2,3-Dihydro-6-hydroxy-7-methoxy-5-benzofurancarboxaldehyde | HCID 21856572 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 6-Hydroxy-7-methoxy-5-benzofurancarboxaldehyde | HCID 21785684 | — |
Reaction Steps
A solution of 817 mg. (3.6 mmole) of DDQ in 10 ml. of dioxane was added to 582 mg. (3 mmole) of 2.3-Dihydro-6-hydroxy-7-methoxy-5-benzofurancarboxaldehyde in 15 ml. of dioxane and the resulting mixture was heated under reflux for 7 hours, cooled and the formed solid removed by filtration. The precipitate was thoroughly washed first with benzene, then with CHCl3. The washings were combined with the initial filtrate and the total concentrated in vacuo to a residue which was chromatographed first on a 20 ml. dry silica gel column (E. Merck 7734) with CHCl3 elution followed by conventional chromatography over 20 g. of silica (E. Merck 7734) packed in benzene-ethyl acetate (95:5) and elution with this solvent mixture provided, after workup, a yellow solid, m.p. 60°-62°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04107182 |
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| Source dataset | uspto-grants-1978_08 |
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| ORD ID | ord-7f35b246bfb64766b166527f289fec84 |
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| Source note | uspto-grants-1978_08 |
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