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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 523032Generated: October 30, 2026

Trifluoroacetic acid → 4-(4-Chlorophenyl)-3,3-dimethylpiperidin-4-ol

https://huagongshe.com/reaction/523032

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant4-(4-Chloro-phenyl)-4-hydroxy-3,3-dimethyl-piperidine-1-carboxylic acid tert-butyl esterHCID 59341212—
SolventDichloromethaneHCID 6344—
Product4-(4-Chlorophenyl)-3,3-dimethylpiperidin-4-olHCID 23131143—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cooled (0° C.) solution of 4-(4-Chloro-phenyl)-4-hydroxy-3,3-dimethyl-piperidine-1-carboxylic acid tert-butyl ester (10.42 g, 30.7 mmol) in methylene chloride (300 mL) was slowly added trifluoroacetic acid (60 mL) over 1.25 hours. The resulting yellow solution was stirred at 0° C. for an additional 1.5 hours. The mixture was concentrated under reduced pressure and the residue dissolved in ethyl acetate (1.2 L), and washed with aqueous sodium hydroxide (1 N, 150 mL). The aqueous layer was extracted with additional ethyl acetate (200 mL) and the combined extracts were washed with brine, dried over sodium sulfate, filtered and concentrated. The resulting solid residue was triturated with ether to afford 4-(4-Chloro-phenyl)-3,3-dimethyl-piperidin-4-ol as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09334283B2
Source datasetuspto-grants-2016_05
ORD IDord-3d8d7b33df134decac2e018ac2b9b03a
Source noteuspto-grants-2016_05