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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371736Generated: October 31, 2026

Ethanol → Ethyl 6,7-dichloro-2,3-dihydro-1-benzofuran-2-carboxylate

https://huagongshe.com/reaction/371736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSulfuric AcidHCID 1118—
Reactant6,7-dichloro-2,3-dihydrobenzofuran-2-carboxylic AcidHCID 9816065—
ProductEthyl 6,7-dichloro-2,3-dihydro-1-benzofuran-2-carboxylateHCID 12747889—

Reaction Steps

A solution of 6,7-dichloro-2,3-dihydrobenzofuran-2-carboxylic acid (70 g.) conc. sulfuric acid (2 ml.) and ethanol (250 ml.) is refluxed for 2 hours. The ethanol is distilled at reduced pressure and the residue is suspended in saturated sodium bicarbonate and extracted with ether. The ether solution is washed with brine, dried over magnesium sulfate and the ether distilled at reduced pressure. The 6,7-dichloro-2,3-dihydrobenzofuran-2-carboxylic acid ethyl ester is used without further purification in the following synthesis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04087542
Source datasetuspto-grants-1978_05
ORD IDord-cc9314e18d464b13b943535600fb6160
Source noteuspto-grants-1978_05