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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromodifluoroacetateHCID 69585—
Reactant1-(4-(5-Fluoropyridin-2-yl)phenyl)ethanoneHCID 59161948—
ReactantHCID 178506586HCID 178506586—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2,2-difluoro-3-[4-(5-fluoropyridin-2-yl)phenyl]-3-hydroxybutanoateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193228B2
Source datasetuspto-grants-2012_06
ORD IDord-fa34da50d3594135831c5b413bedfab8
Source noteuspto-grants-2012_06