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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591053Generated: October 30, 2026

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

https://huagongshe.com/reaction/591053

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl (4-bromo-2,5-dimethyl-thiophen-3-yl)-oxo-acetateHCID 70818387—
ReactantSodium tetraborohydrideHCID 131720822—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-(4-bromo-2,5-dimethylthiophen-3-yl)-2-hydroxyacetateHCID 7081871489%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of ethyl 2-(4-bromo-2,5-dimethylthiophen-3-yl)-2-oxoacetate (28c) (1 g, 3.56 mmol) in tetrahydrofuran (22.5 mL) and ethanol (5.6 mL) cooled to 0° C. is added sodium tetraborohydride (121.2 mg, 3.20 mmol). The mixture is stirred at 0° C. for 1 hour. The mixture is quenched with HCl (1N) and extracted with ethyl acetate. The organic extract is washed with brine, dried over sodium sulfate, filtered and concentrated to afford the desired alcohol (28d) as a white solid (836 mg, 2.85 mmol, 89%) which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238026B2
Source datasetuspto-grants-2016_01
ORD IDord-f30e2234a6f64b6dbc1c2ebc1f2daa16
Source noteuspto-grants-2016_01