HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 590974Generated: October 26, 2026
Sodium borohydride → Ethyl 2-(3,5-dibromothiophen-2-yl)-2-hydroxyacetate
https://huagongshe.com/reaction/590974
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Ethyl 3,5-dibromo-alpha-oxo-2-thiopheneacetate | HCID 14113379 | — |
| Catalyst | Hydrochloric Acid | HCID 313 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 2-(3,5-dibromothiophen-2-yl)-2-hydroxyacetate | HCID 70818161 | 75% |
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 (7a) (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 ethyl 2-(3,5-dibromothiophen-2-yl)-2-hydroxyacetate (0.32 g, 0.93 mmol, 75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09238026B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-88f25726527049dc93b7dbc2ad5be62e |
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| Source note | uspto-grants-2016_01 |
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