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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 556945Generated: October 30, 2026

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

https://huagongshe.com/reaction/556945

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 numberUS08058287B2
Source datasetuspto-grants-2011_11
ORD IDord-97d21c3eaeb44b02b6ad841d1037529d
Source noteuspto-grants-2011_11