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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354029Generated: October 31, 2026

p-Toluenesulfonic acid → 1-(4-Hydroxyphenyl)-4-(4-trifluoromethoxyphenoxy)piperidine p-toluenesulfonate

https://huagongshe.com/reaction/2354029

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantTriethylamineHCID 8471—
Reactant1,4-CyclohexanedioneHCID 12511—
Reactant4-[4-(Trifluoromethoxy)phenoxy]piperidineHCID 16115439—
SolventEthanolHCID 702—
Product1-(4-Hydroxyphenyl)-4-(4-trifluoromethoxyphenoxy)piperidine p-toluenesulfonateHCID 86615244—

Reaction Steps

100 mg of 4-(4-trifluoromethoxyphenoxy)piperidine, 64 mg of 1,4-cyclohexanedione and 0.02 ml of triethylamine were heated in 15 ml of ethanol and reacted at 50° C. to 60° C. for 6 hours. After the completion of the reaction, the reaction mixture was concentrated under reduced pressure and ethyl acetate was added thereto to prepare an ethyl acetate solution, to which p-toluenesulfonic acid was added. After leaving at room temperature for 30 minutes, the precipitate was filtrated and washed with ethyl acetate. The obtained crystal was air-dried and 139 mg of 1-(4-hydroxyphenyl)-4-(4-trifluoromethoxyphenoxy)piperidine p-toluenesulfonate was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07750156B2
Source datasetuspto-grants-2010_07
ORD IDord-8658746fbf204094ae690d4538a78d1e
Source noteuspto-grants-2010_07