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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2185485Generated: October 29, 2026

Trifluoroacetic acid → 4-(2-Chloro-5-methylphenoxy)piperidine

https://huagongshe.com/reaction/2185485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactantn-Tert-butoxycarbonyl-4-(2-chloro-5-methylphenoxy)piperidineHCID 22458419—
SolventDichloromethaneHCID 6344—
Product4-(2-Chloro-5-methylphenoxy)piperidineHCID 17195100—

Reaction Steps

Trifluoroacetic acid (6 mL) was added to a solution of N-tert-butoxycarbonyl-4-(2-chloro-5-methylphenoxy)piperidine (A, 489 mg) in dichloromethane (20 mL) at room temperature. After stirring at room temperature for 30 min, the reaction mixture was evaporated in vacuo. The residue was partitioned between chloroform and saturated sodium hydrogen carbonate. The organic layer was dried over anhydrous sodium sulfate and then concentrated in vacuo to give the titled compound as yellow crystals, which was used in the next reaction without her purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06399629B1
Source datasetuspto-grants-2002_06
ORD IDord-9341a83b03f24b8db2017f6ac3f78e00
Source noteuspto-grants-2002_06