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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2051659Generated: October 31, 2026

2-Furancarbonyl chloride → HCID 12747893, compound

https://huagongshe.com/reaction/2051659

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Furancarbonyl chlorideHCID 68242—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant6,7-dichloro-2,3-dihydrobenzofuran-2-carboxylic AcidHCID 9816065—
SolventDichloromethaneHCID 6344—
ProductHCID 12747893HCID 12747893—

Reaction Steps

To a well stirred mixture of 6,7-dichloro-2,3-dihydro-benzofuran-2-carboxylic acid (3.3 g.), furan-2-carbonyl-chloride (3.6 g.) and 200 ml methylene chloride, protected from the atmosphere with a calcium chloride tube is added anhydrous aluminum chloride (3.7 g.) over an one-half hour period. The reaction solution is stirred 18 hours at 25° C. and then refluxed for 1 hour. The solvent is removed and the residue added to ice water (200 ml.) and hydrochloric acid (20 ml.). The product is extracted into ether, washed with water, then extracted into aqueous sodium bicarbonate (200 ml.) from which the sodium salt of the product precipitates. The sodium salt of the product is placed in a separatary funnel with dilute hydrochloric acid (100 ml.) and ether (100 ml.) and shaken until the solid dissolves. The ether solution is washed with water, brine, dried over magnesium sulfate and the ether distilled at reduced pressure. The 6,7-dichloro-2,3-dihydro-5-(2-furoyl) benzofuran-2-carboxylic acid melts at 166° C. after crystallization from acetonitrile/n-butyl chloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04181727
Source datasetuspto-grants-1980_01
ORD IDord-579329d85fb04642a8110929a4494a22
Source noteuspto-grants-1980_01