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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 543421Generated: October 29, 2026

Chloroform → HCID 13650581, compound

https://huagongshe.com/reaction/543421

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantPotassium CarbonateHCID 11430—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 15617028HCID 15617028—
SolventWaterHCID 962—
ProductHCID 13650581HCID 1365058144.9%

Reaction Steps

A mixture of 4-allyl-3-hydroxy-1-methyl-9-oxo-9H-xanthene (3.0 g), m-chloroperbenzoic acid (8 g) and chloroform (500 ml) was stirred at room temperature for 5 hours and thereafter left to stand overnight. To the mixture, potassium carbonate (20 g) and water (400 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 (500 ml) and, to the stirred solution, a mixture of chromium trioxide (5.5 g), water (25 ml) and concentrated sulfuric acid (8.5 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 1.5 g of 1,2-dihydro-5-methyl-6-oxo-6H-furo[2,3-c]xanthene-2-carboxylic acid. m.p. 231°-234° C. This compound exhibited a mass spectrum having a molecular ion peak at m/e 298.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04661607
Source datasetuspto-grants-1987_04
ORD IDord-bfccbfe9995d40c1a312d2e2050cdd55
Source noteuspto-grants-1987_04