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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1653807Generated: October 31, 2026

Water → HCID 19972719, compound

https://huagongshe.com/reaction/1653807

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSulfuric AcidHCID 1118—
ReactantPotassium PermanganateHCID 516875—
ReactantSodium PyrosulfiteHCID 656671—
Reactant4H-1-BENZOPYRAN-4-ONE, 3-METHYL-2-PHENYL-8-(2-PRHCID 23275621—
CatalystTrioctylmethylammonium chlorideHCID 21218—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
ProductHCID 19972719HCID 19972719—

Reaction Steps

4.5 g of potassium permanganate was added portionwise within 1.5 hours under stirring at 0°-10° C., to a mixture of 2.76 g of 8-allyl-3-methyl-4-oxo-2-phenyl-4H-1-benzopyran (P. Da Re, U.S. Pat. No. 3,350,411), 0.17 g of Aliquat 336, 1.12 ml of acetic acid, 56 ml of dichloromethane, 3.2 ml of sulfuric acid (d=1.84) and 60 ml of water. Stirring was continued at room temperature for 5 hours. 3.4 g of sodium metabisulfite were added portionwise at 0°-5° C. within 15 minutes. The organic layer was separated, washed with water and extracted with 60 ml of 1N aqueous sodium hydroxide solution. The aqueous phase was acidified by addition of diluted hydrochloric acid and extracted with ethyl acetate. The organic phase was washed with water, dried on anhydrous sodium sulfate and, after filtration, evaporated to dryness in vacuo. The residue was treated with carbon tetrachloride and the solid was collected by suction to give 1 g of the title compound, m.p. 191°-192° C. (acetonitrile).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05403842
Source datasetuspto-grants-1995_04
ORD IDord-064e6f751f8f4dffa0864fa27c82c9ec
Source noteuspto-grants-1995_04