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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242563Generated: October 27, 2026

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

https://huagongshe.com/reaction/242563

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 numberUS08653096B2
Source datasetuspto-grants-2014_02
ORD IDord-92aae535003c45c2a748a8c53874f5ce
Source noteuspto-grants-2014_02