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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 410313Generated: October 29, 2026

HCID 59326823, compound → HCID 59326798, compound

https://huagongshe.com/reaction/410313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59326823HCID 59326823—
ReactantHCID 178418573HCID 178418573—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59326798HCID 59326798—

Reaction Steps

To a solution of 3-(2-fluoropyridin-3-yl)cyclopent-2-enone (1 g, 5.64 mmol) in THF (28.2 mL) was added methylmagnesium bromide (4.70 mL, 14.11 mmol) dropwise over 5 minutes. The dark brown solution was stirred for 3 h at room temperature before. slowly quenching with aqueous ammonium chloride. The crude reaction was diluted with water and extracted with ethyl acetate, drying over magnesium sulfate, filtering, and concentrating to a dark brown oil under reduced pressure. The crude compound was purified by column chromatography (ethyl acetate/dichloromethane) to afford 3-(2-fluoropyridin-3-yl)-1-methylcyclopent-2-enol as a clear oil. MS (ESI, pos. ion) m/z: 194.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759532B2
Source datasetuspto-grants-2014_06
ORD IDord-76b6d69ef1154c7fa18696d1876db697
Source noteuspto-grants-2014_06