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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591020Generated: October 31, 2026

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

https://huagongshe.com/reaction/591020

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 7081838739.3%

Reaction Steps

Under a nitrogen atmosphere, aluminium chloride (1.46 g, 11 mmol) was added per portions at 0° C. to a solution of 3-bromo-2,5-dimethylthiophene (17b) (1.05 g, 5.49 mmol) and ethyl chlorooxoacetate (614 μL, 5.5 mmol) in dichloromethane (12 mL). After 2 hours of vigorous stirring, the reaction mixture was slowly hydrolyzed at 0° C. with water. The organic layer was separated, washed with hydrochloric acid aqueous solution 1N, 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 afford the desired keto-ester (17c) as a orange solid (630 mg, 2.16 mmol, 39%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238026B2
Source datasetuspto-grants-2016_01
ORD IDord-2143aba0159240bdbf63960d01126530
Source noteuspto-grants-2016_01