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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 543418Generated: October 30, 2026

Chloroform → HCID 13650573, compound

https://huagongshe.com/reaction/543418

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantPotassium CarbonateHCID 11430—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 15617023HCID 15617023—
SolventWaterHCID 962—
ProductHCID 13650573HCID 1365057340.7%

Reaction Steps

A mixture of 2-allyl-4-chloro-3-hydroxy-9-oxo-9H-xanthene (2.0 g), m-chloroperbenzoic acid (3.6 g) and chloroform (100 ml) was stirred at room temperature for 5 hours and thereafter left to stand overnight. To the mixture, potassium carbonate (8 g) and water (200 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 (400 ml) and to the stirred solution, a mixture of chromium trioxide (1.7 g), water (10 ml) and concentrated sulfuric acid (3 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 0.9 g of 11-chloro-2,3-dihydro-5-oxo-5H-furo[3,2-b]xanthene-2-carboxylic acid. m.p. 290°-293° C. This compound exhibited a mass spectrum having a molecular ion peak at m/e 316.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04661607
Source datasetuspto-grants-1987_04
ORD IDord-4fd353255a2f4633a798d8191c38be6f
Source noteuspto-grants-1987_04