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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837723Generated: November 2, 2026

Hydrochloride methanol → (E)-4-[2-(2-fluorophenyl)vinyl]piperidine

https://huagongshe.com/reaction/1837723

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloride methanolHCID 21893726—
Reactant1-(vinyloxycarbonyl)-4-[(E)-2-(2-fluorophenyl)-1-ethenyl]piperidineHCID 22678783—
Product(E)-4-[2-(2-fluorophenyl)vinyl]piperidineHCID 2224826997.9%

Reaction Steps

904 mg of 1-(vinyloxycarbonyl)-4-[(E)-2-(2-fluorophenyl)-1-ethenyl]piperidine was suspended in 5 ml of a 10% hydrogen chloride-methanol solution. After stirring for 15 minutes at room temperature, the mixture was heated at 70° C. for one hour. The solvent was evaporated, and water and ethyl acetate were added to the residue, to separate the aqueous layer. The aqueous layer was basified with a diluted ammonia, and extracted with ethyl acetate. The organic layer was washed with water and brine, and then dried over anhydrous magnesium sulfate. The solvent was evaporated, to give 660 mg of the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06784192B2
Source datasetuspto-grants-2004_08
ORD IDord-b1437d05714c4e428c6059b7aab18ff2
Source noteuspto-grants-2004_08