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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010873Generated: October 30, 2026

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

https://huagongshe.com/reaction/1010873

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 numberUS07977350B2
Source datasetuspto-grants-2011_07
ORD IDord-5b0ebebe08fc47c883b67a161238cc7e
Source noteuspto-grants-2011_07