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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29414Generated: October 29, 2026

Acetyl chloride → Ethyl 5-acetyl-4-hydroxy-3-methylbenzofuran-2-carboxylate

https://huagongshe.com/reaction/29414

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantEthyl 4-hydroxy-3-methyl-1-benzofuran-2-carboxylateHCID 748649—
CatalystTitanium TetrachlorideHCID 24193—
SolventChlorobenzeneHCID 7964—
ProductEthyl 5-acetyl-4-hydroxy-3-methylbenzofuran-2-carboxylateHCID 2020510159%

Reaction Steps

To 4-hydroxy-3-methyl-benzofuran-2-carboxylic acid ethyl ester 0.5 g (2.27 mmol) was added 15 mL of chlorobenzene, 0.27 g (3.4 mmol) of acetyl chloride and 0.63 mL (5.7 mmol) of titanium tetrachloride. The mixture was sealed in a pressure tube and the tube was placed in 95° C. oil bath for 5 h with stirring. The reaction mixture was washed with 0.5N HCl and was extracted with ethyl acetate. Removal of the solvents gave the crude product, which was purified by column chromatography to give 0.33 g (59% yield) of 5-acetyl-4-hydroxy-3-methyl-benzofuran-2-carboxylic acid ethyl ester as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07420001B2
Source datasetuspto-grants-2008_09
ORD IDord-2be44430397b41dab8f07180b2815339
Source noteuspto-grants-2008_09