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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1194870Generated: November 4, 2026

Chloroform → HCID 13650584, compound

https://huagongshe.com/reaction/1194870

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantPotassium CarbonateHCID 11430—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 15617030HCID 15617030—
SolventWaterHCID 962—
ProductHCID 13650584HCID 1365058465.2%

Reaction Steps

A mixture of 4-allyl-3-hydroxy-2-methyl-9-oxo-9H-xanthene (12 g), m-chloroperbenzoic acid (12 g) and chloroform (700 ml) was stirred at room temperature for 5 hours and thereafter left to stand overnight. To the mixture, 20 g of potassium carbonate and 400 ml of water were added and the resulting mixture was extracted with chloroform. The chloroform layer was dried and the solvent was distilled off. The residue was dissolved in acetone (2,000 ml) and, to the stirred solution, a mixture of chromium trioxide (34 g), water (70 ml) and concentrated sulfuric acid (30 ml) was added dropwise at room temperature. After standing overnight, the mixture was filtered and the filtrate was evaporated to dryness under vacuum. After addition of water, the solid crystal was recovered by filtration, washed with water and dried. Recrystallization from a mixed solvent of ethanol and DMF gave 8.7 g of 1,2-dihydro-4-methyl-6-oxo-6H-furo[2,3-c]xanthene-2-carboxylic acid. m.p. 292°-295° C. This compound produced a mass spectrum having a molecular ion peak at m/e 296.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04816479
Source datasetuspto-grants-1989_03
ORD IDord-7c8b7407d440489a917685c6939319f6
Source noteuspto-grants-1989_03