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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242580Generated: October 27, 2026

Trifluoroacetic acid → 4-(4-Chlorophenyl)-4-methoxy-3-methyl-3-piperidinol

https://huagongshe.com/reaction/242580

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 66757870HCID 66757870—
SolventDichloromethaneHCID 6344—
Product4-(4-Chlorophenyl)-4-methoxy-3-methyl-3-piperidinolHCID 23136865—

Reaction Conditions

Temperature0 °C

Reaction Steps

4-(4-Chloro-phenyl)-3-hydroxy-4-methoxy-3-methyl-piperidine-1-carboxylic acid tert-butyl ester (260 mg, 0.74 mmol) was dissolved in methylene chloride (5 mL) and the resulting solution was cooled to 0° C. Trifluoroacetic acid (1 mL) was added and the mixture was stirred 2 h. Solvents were then removed under reduced pressure and the residue dissolved in ethyl acetate. Water and 6 N aqueous sodium hydroxide were added until the pH=10. The organic phase was washed with brine and dried over magnesium sulfate, filtered and concentrated to afford 4-(4-chloro-phenyl)-4-methoxy-3-methyl-piperidin-3-ol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653096B2
Source datasetuspto-grants-2014_02
ORD IDord-0f76fd2820e44897acaca4811e420833
Source noteuspto-grants-2014_02