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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 395055Generated: October 29, 2026

3-Methyl-but-2-enoic acid 4-bromo-phenyl ester → 2H-1-Benzopyran-2-one, 6-bromo-3,4-dihydro-4,4-dimethyl-

https://huagongshe.com/reaction/395055

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Methyl-but-2-enoic acid 4-bromo-phenyl esterHCID 733797—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
Product2H-1-Benzopyran-2-one, 6-bromo-3,4-dihydro-4,4-dimethyl-HCID 2256892359.7%

Reaction Steps

A solution of 3-methyl-but-2-enoic acid 4-bromo-phenyl ester (7 g, 27.6 mmol) in anhydrous dichloromethane (200 mL) was cooled (ice bath) and treated with aluminum chloride (6.6 g, 49.6 mmol) and the reaction mixture was stirred overnight at ambient temperature. The reaction mixture was quenched with saturated aqueous sodium bicarbonate solution and extracted with diethyl ether (×2). The combined organic extract was washed woth brine (×1), dried over anhydrous sodium sulfate, filtered and evaporated in vacuo to afford an oil which was purified by flash column chromatography over silica gel (230-400 mesh) using 2.5% ethyl acetate in hexane as the eluent to afford the title compound (4.2 g, 57%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06603019B2
Source datasetuspto-grants-2003_08
ORD IDord-9ee50011cfb149668dce74301ed7c226
Source noteuspto-grants-2003_08