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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 590985Generated: October 26, 2026

Sodium borohydride → Ethyl 2-(3,5-dibromothiophen-2-yl)-2-hydroxyacetate

https://huagongshe.com/reaction/590985

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantEthyl 3,5-dibromo-alpha-oxo-2-thiopheneacetateHCID 14113379—
CatalystHydrochloric AcidHCID 313—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-(3,5-dibromothiophen-2-yl)-2-hydroxyacetateHCID 7081816175%

Reaction Conditions

Temperature-10 °C

Reaction Steps

Under a nitrogen atmosphere, sodium borohydride (0.14 g, 3.7 mmol) was added portionwise to a solution of ethyl 2-(3,5-dibromothiophen-2-yl)-2-oxoacetate (10a) (0.42 g, 1.24 mmol) in anhydrous tetrahydrofuran (10 mL), previously cooled to −10° C. After 30 minutes stirring, a few drops of 1 M hydrochloric acid were added and the resulting precipitate was filtered. The filtrate was concentrated in vavuo. The residue was dissolved in brine, and extracted with ethyl acetate (2×20 mL). The organic layer was dried over sodium sulfate, filtered, and evaporated to dryness. The residue was purified by flash chromatography on silica gel (cyclohexane/ethyl acetate 80/20) to provide the desired alcohol (10b) (0.32 g, 0.93 mmol, 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238026B2
Source datasetuspto-grants-2016_01
ORD IDord-cca818d6b29c452482a7916ebcd2503b
Source noteuspto-grants-2016_01