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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1194863Generated: November 2, 2026

Chloroform → HCID 13650576, compound

https://huagongshe.com/reaction/1194863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantPotassium CarbonateHCID 11430—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant3-Hydroxy-4-(prop-2-en-1-yl)-9H-xanthen-9-oneHCID 12529205—
SolventWaterHCID 962—
ProductHCID 13650576HCID 1365057635.8%

Reaction Steps

A mixture of 4-allyl-3-hydroxy-9-oxo-9H-xanthene (10 g), m-chloroperbenzoic acid (21 g) and chloroform (1,000 ml) was stirred at room temperature for 5 hours and thereafter left to stand overnight. To the mixture, potassium carbonate (40 g) and water (1,000 ml) 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 (9 g), water (40 ml) and concentrated sulfuric acid (15 g) 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 ethanol gave 4 g of 1,2-dihydro-6-oxo-6H-furo[2,3-c]xanthene-2-carboxylic acid. m.p. 283°-286° C. This compound showed a mass spectrum having a molecular ion peak at m/e 282.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04816479
Source datasetuspto-grants-1989_03
ORD IDord-c82e11c54599469481256a90af789922
Source noteuspto-grants-1989_03