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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1194869Generated: November 3, 2026

Chloroform → HCID 13650583, compound

https://huagongshe.com/reaction/1194869

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantPotassium CarbonateHCID 11430—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 13025300HCID 13025300—
SolventWaterHCID 962—
ProductHCID 13650583HCID 1365058345.8%

Reaction Steps

A mixture of 4-allyl-2-bromo-3-hydroxy-9-oxo-9H-xanthene (3.0 g), m-chloroperbenzoic acid (10 g) and chloroform (250 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 distilled off. The residue was dissolved in acetone (300 ml) and, to the stirred solution, a mixture of chromium trioxide (5 g), water (25 ml) and concentrated sulfuric acid (8 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 4-bromo-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 360.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04816479
Source datasetuspto-grants-1989_03
ORD IDord-0ac6c486dfc84e4197f62b2758a1f489
Source noteuspto-grants-1989_03