Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1756028Generated: October 28, 2026

m-Chloroperbenzoic acid → Ethyl 7-acetoxy-2,3-dihydro-1,4-benzodioxin-2-carboxylate

https://huagongshe.com/reaction/1756028

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantEthyl 7-acetyl-2,3-dihydro-1,4-benzodioxine-2-carboxylateHCID 13723676—
SolventDichloromethaneHCID 6344—
ProductEthyl 7-acetoxy-2,3-dihydro-1,4-benzodioxin-2-carboxylateHCID 1085839575%

Reaction Steps

Heat a solution of 2 g (8 mmol) of ethyl 7-acetyl-2,3-dihydro-1,4-benzodioxin-2-carboxylate and 3.05 g (17.7 mmol) of meta-chloro-perbenzoic acid in 30 cm3 of methylene chloride at 50° C. for 18 hours under a nitrogen atmosphere. After cooling, removing by filtration the benzoic acid formed, and washings with aqueous solutions of sodium hydrogen carbonate and then sodium chloride, the reaction mixture is concentrated to dryness under reduced pressure and the crude product obtained is purified by chromatography on a silica column (eluant: petroleum ether/diethyl ether, 70:30). Ethyl 7-acetoxy-2,3-dihydro-1,4-benzodioxin-2-carboxylate is thereby obtained in a yield of 75%. ##STR36##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05439909
Source datasetuspto-grants-1995_08
ORD IDord-29264e5ad25b45c0b7b59e8908aa3721
Source noteuspto-grants-1995_08