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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066852Generated: October 31, 2026

Trifluoroacetic acid → 3-[2-(2-Fluoro-5-bromobenzyloxy)ethyl]piperidine

https://huagongshe.com/reaction/1066852

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant1-(t-Butoxycarbonyl)-3-[2-(2-fluoro-5-bromobenzyloxy)ethyl]piperidineHCID 21196136—
SolventDichloromethaneHCID 6344—
Product3-[2-(2-Fluoro-5-bromobenzyloxy)ethyl]piperidineHCID 21196120—

Reaction Conditions

Temperature0 °C

Reaction Steps

In a 1-ml round bottom flask 1-(t-butoxycarbonyl)-3-[2-(2-fluoro-5-bromobenzyloxy)ethyl]piperidine (0.495 g) was dissolved in methylene chloride (4 ml) under a nitrogen atmosphere. The solution was cooled to 0° C. and trifluoroacetic acid (1 ml) was slowly added dropwise. The resulting mixture was stirred for thirty minutes at ambient temperature. The progress of the reaction was monitored by thin layer chromatography. The reaction mixture was partitioned between 1 M potassium carbonate and methylene chloride. The aqueous fraction was back extracted with methylene chloride. The organic fractions were combined, and dried over sodium sulfate. The solvents were removed in vacuo. The resulting residue was used as is.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06245761B1
Source datasetuspto-grants-2001_06
ORD IDord-66e0ef759dcc42a28d4664241a88bf9b
Source noteuspto-grants-2001_06