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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1667316Generated: November 2, 2026

tert-butyl 4-[(E)-2-(2-chloro-6-methylphenyl)vinyl]piperidine-1-carboxylate → 4-[(E)-2-(2-chloro-6-methylphenyl)vinyl]piperidine hydrochloride

https://huagongshe.com/reaction/1667316

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl 4-[(E)-2-(2-chloro-6-methylphenyl)vinyl]piperidine-1-carboxylateHCID 10088346—
SolventEthanolHCID 702—
SolventEthanol hydrochlorideHCID 21887872—
Product4-[(E)-2-(2-chloro-6-methylphenyl)vinyl]piperidine hydrochlorideHCID 67443669144.2%

Reaction Steps

To a solution of 645 mg of tert-butyl 4-[(E)-2-(2-chloro-6-methylphenyl)vinyl]piperidine-1-carboxylate in 4 ml of ethanol, 3 ml of 35% hydrogen chloride-ethanol was added, followed by stirring at ambient temperature for 5 hours. The reaction mixture was evaporated under reduced pressure and the residue was azeotropically distilled with 5 ml of toluene 3 times to give crystals. The collected crystals were recrystallized from ethanol-ethyl acetate to give 377 mg of 4-[(E)-2-(2-chloro-6-methylphenyl)vinyl]piperidine hydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044206B2
Source datasetuspto-grants-2011_10
ORD IDord-abf4fa44d5654b9f929efb49f9d3d6cf
Source noteuspto-grants-2011_10