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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 269916Generated: October 25, 2026

Tetrahydrofuran → 1-(2,5-Difluoro-4-methoxyphenyl)-4-methoxymethylenepiperidine

https://huagongshe.com/reaction/269916

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantMethoxymethyl-triphenylphosphonium chlorideHCID 2723798—
Reactant1-(2,5-Difluoro-4-methoxyphenyl)piperidin-4-oneHCID 23111466—
SolventWaterHCID 962—
Product1-(2,5-Difluoro-4-methoxyphenyl)-4-methoxymethylenepiperidineHCID 2311140034.1%

Reaction Steps

A reaction vessel was charged with methoxymethyltriphenyl-phosphonium chloride (1.114 g), the atomosphere indide the vessel was substituted with nitrogen, and anhydrous tetrahydrofuran (2 mL) was added, followed by further dropwise addition of 1.57 M n-butyl lithium-in-hexane solution (2 mL) at room temperature and thereafter 10 minutes' stirring at room temperature. To the reaction mixture a mixture of 1-(2,5-difluoro-4-methoxyphenyl)piperidin-4-one (676 mg) and anhydrous tetrahydrofuran (0.5 mL) was added dropwise, followed by 30 minutes' stirring at room temperature. To the reaction mixture water was added, followed by extraction with ethyl acetate. The organic layer was washed with saturated saline solution and dried over anhydrous sodium sulfate. Distilling the solvent off, the crude product as obtained was purified on silica gel column chromatography (eluent, hexane: ethyl acetate=10:1) to provide 1-(2,5-difluoro-4-methoxyphenyl)-4-methoxymethylenepiperidine (257 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07449466B2
Source datasetuspto-grants-2008_11
ORD IDord-0354f4e12ffe4f7cad2355f89c6f816a
Source noteuspto-grants-2008_11