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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 363465Generated: October 30, 2026

m-Chloroperbenzoic acid → HCID 21831345, compound

https://huagongshe.com/reaction/363465

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 21831331HCID 21831331—
SolventDichloromethaneHCID 6344—
ProductHCID 21831345HCID 2183134544.5%

Reaction Steps

A mixture of 3.1 g of 2,2-bisfluoromethyl-6-heptafluoropropyl-2H-1-benzopyran, 4.20 g of m-chloroperbenzoic acid (70%) and 50 ml of methylene chloride was stirred at room temperature for 27 hours. After removal of the separated crystal by filtration, the filtrate was washed with saturated sodium hydrogen carbonate solution and saturated saline'solution, and dried with sodium sulfate. The solvent was distilled off and the resultant residue was purified using silica gel column chromatography (developing solution, hexane:CH2Cl2 =5:1) to obtain 1.44 g of oily 3,4-epoxy-2,2-bisfluoromethyl-6-heptafluoropropyl-3,4-dihydro-2H-1-benzopyran represented by the following formula.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05874446
Source datasetuspto-grants-1999_02
ORD IDord-6c331cce49f14e72a6aeefef817162c8
Source noteuspto-grants-1999_02