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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 457078Generated: October 27, 2026

1,4-Dioxane hydrochloride → 4-(4-Chlorophenyl)-3,3-dimethylpiperidin-4-ol

https://huagongshe.com/reaction/457078

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-Dioxane hydrochlorideHCID 20443148—
Reactant4-(4-Chloro-phenyl)-4-hydroxy-3,3-dimethyl-piperidine-1-carboxylic acid tert-butyl esterHCID 59341212—
Product4-(4-Chlorophenyl)-3,3-dimethylpiperidin-4-olHCID 23131143—

Reaction Steps

4-(4-Chloro-phenyl)-4-hydroxy-3,3-dimethyl-piperidine-1-carboxylic acid tert-butyl ester (0.25 g, 0.73 mmol) was dissolved in 4M HCl/Dioxane (2 mL, 8 mmol). The solution was stirred at room temperature for about 4 hours. The solvent was removed in vacuo. The residue was quenched with aqueous sodium hydroxide, extracted with ethyl acetate, and the organic layers were dried over sodium sulfate and evaporated in vacuo to yield the title compound as a yellow solid. The mixture was carried on to the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07186729B2
Source datasetuspto-grants-2007_03
ORD IDord-ed717ada9fa8481497f0a2b3bb014859
Source noteuspto-grants-2007_03