HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 216373Generated: October 25, 2026
Ethyl bromodifluoroacetate → Ethyl 2,2-difluoro-3-[4-(5-fluoropyridin-2-yl)phenyl]-3-hydroxybutanoate
https://huagongshe.com/reaction/216373
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromodifluoroacetate | HCID 69585 | — |
| Reactant | 1-(4-(5-Fluoropyridin-2-yl)phenyl)ethanone | HCID 59161948 | — |
| Reactant | HCID 178506586 | HCID 178506586 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 2,2-difluoro-3-[4-(5-fluoropyridin-2-yl)phenyl]-3-hydroxybutanoate | HCID 68667425 | — |
Reaction Steps
A solution of ethyl bromo(difluoro)acetate (0.53 mL, 4.1 mmol) and 1-[4-(5-fluoropyridin-2-yl)phenyl]ethanone (800 mg, 3.7 mmol) in tetrahydrofuran (40 mL) was added to a 0.1 M solution of samarium diiodide in tetrahydrofuran (82 mL, 8.2 mmol) at ambient temperature. After stirring at ambient temperature for 3 min, the reaction was cooled and quenched with 1N aqueous hydrochloric acid. Volatiles were removed in vacuo and the residue was partitioned between ethyl acetate and 1 N hydrochloric acid. The organic phase was washed with saturated aqueous sodium bicarbonate and brine, dried (sodium sulfate) and concentrated in vacuo. Chromatography over silica eluting with 0-40% ethyl acetate/hexane afforded ethyl 2,2-difluoro-3-[4-(5-fluoropyridin-2-yl)phenyl]-3-hydroxybutanoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08193228B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-fa34da50d3594135831c5b413bedfab8 |
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| Source note | uspto-grants-2012_06 |
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