HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 66079Generated: October 25, 2026
Water → 2-hydroxy-9-methoxy-5-methyl-2,3-dihydro-7H-furo[3,2-g][1]benzopyran-7-one
https://huagongshe.com/reaction/66079
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Potassium periodate | HCID 516896 | — |
| Reactant | 7-Hydroxy-8-methoxy-4-methyl-6-(prop-2-en-1-yl)-2H-1-benzopyran-2-one | HCID 21814502 | — |
| Catalyst | Osmium Tetroxide | HCID 30318 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-hydroxy-9-methoxy-5-methyl-2,3-dihydro-7H-furo[3,2-g][1]benzopyran-7-one | HCID 20380227 | — |
Reaction Steps
A solution of 2.0 g (8.12 mmols) of 6-allyl-7-hydroxy-8-methoxy-4-methylcoumarin in 20 ml of methanol was treated (mechanical stirring) with 10 ml of water, 5.0 g potassium periodate, and 1.0 ml of a 10% aqueous solution of osmium tetroxide (10 mg/ml). After 3.5 hrs, the mixture was partitioned between water/methylene chloride. The aqueous phase was further extracted with methylene chloride. The organic extracts were dried and evaporated to yield 2-hydroxy-9-methoxy-5-methyl-2,3-dihydro-7H-furo[3,2-g][1]benzopyran-7-one. The compound was dissolved in 40 ml of 98% formic acid and heated under reflux for 1.0 hr. The solution was cooled and evaporated to dryness. The residue was chromatographed over silica, eluting with ethyl acetate/benzene, 1:4, to afford pure 9-methoxy-5-methyl-7H-furo[3,2-g][1]benzopyran-7-one, m.p. 167°-168° (ethanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04130568 |
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| Source dataset | uspto-grants-1978_12 |
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| ORD ID | ord-7e625edc8b3846789c622aabd8df2edf |
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| Source note | uspto-grants-1978_12 |
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