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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 511071Generated: October 31, 2026

Hydrochloric Acid → 1-[4-(Trifluoromethyl)phenyl]piperidin-4-ol

https://huagongshe.com/reaction/511071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
ReactantBenzene, 1-bromo-4-(trifluoromethyl)-HCID 67872—
ReactantPiperidin-4-olHCID 79341—
ReactantSodium BicarbonateHCID 516892—
ReactantDicyclohexyl-(1-methyl-2-phenylcyclohexa-2,4-dien-1-yl)phosphaneHCID 66672255—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Product1-[4-(Trifluoromethyl)phenyl]piperidin-4-olHCID 22097674—

Reaction Conditions

Temperature65 °C

Reaction Steps

A mixture of 4-hydroxypiperidine (100 mg; 0.99 mmol), 4-bromo benzotrifluoride (0.167 mL, 1.19 mmol), tris(dibenzylideneacetone)dipalladium (37 mg; 0.04 mmol) and 2-(dicyclohexylphosphino)-2-methylbiphenyl (29 mg; 0.08 mmol) is thoroughly flushed with argon and tetrahydrofuran is added (1 mL). A molar solution of bis-(trimethylsilyl)-lithium amide in tetrahydrofuran (1.9 mL, 1.90 mmol) is added and the reaction mixture is heated at 65° C. After 17 hours reaction time, aq. 1M hydrochloric acid (7.5 mL) is added and the mixture is stirred for 15 minutes before neutralization by addition of aq. sat. sodium hydrogencarbonate. The mixture is extracted with ethyl acetate (2×10 mL). The combined organic layers are dried over sodium sulfate, filtered and evaporated under reduced pressure to yield crude 1-(4-trifluoromethyl-phenyl)-piperidin-4-ol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096524B2
Source datasetuspto-grants-2015_08
ORD IDord-a623f685b8a24c1da5683b907081a0dd
Source noteuspto-grants-2015_08