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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591052Generated: October 30, 2026

Water → Ethyl (4-bromo-2,5-dimethyl-thiophen-3-yl)-oxo-acetate

https://huagongshe.com/reaction/591052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthoxalyl chlorideHCID 20884—
Reactant3-Bromo-2,5-dimethylthiopheneHCID 638585—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
ProductEthyl (4-bromo-2,5-dimethyl-thiophen-3-yl)-oxo-acetateHCID 7081838753.9%

Reaction Steps

Under a nitrogen atmosphere, ethyl chlorooxoacetate (1.04 mL, 9.27 mmol) and aluminum chloride (per 3 portions) (2.47 g, 18.54 mmol) was added successively at −5° C. to a solution of 3-bromo-2,5-dimethylthiophene (28b) (886 mg, 4.64 mmol) in dichloromethane (20 mL). After 3 hours at −5° C., the reaction mixture was slowly hydrolyzed at 0° C. with water. The organic layer was separated, washed with water, brine, dried over sodium sulfate, filtered, and evaporated under reduced pressure. The residue was purified by flash chromatography on silica gel (cyclohexane/ethyl acetate 95/5) to give the desired keto-ester (28c) (725 mg, 2.50 mmol, 50%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238026B2
Source datasetuspto-grants-2016_01
ORD IDord-6331ce2500664e8f851c411d6d42fd3f
Source noteuspto-grants-2016_01