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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419570Generated: November 3, 2026

Trifluoroacetic acid methylene chloride → tert-Butyl 4-(2-aminophenyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1419570

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acid methylene chlorideHCID 21863450—
Reactantt-Butyl (1-t-Butoxycarbonylpiperidin-4-yl)phenylcarbamateHCID 54392086—
Producttert-Butyl 4-(2-aminophenyl)piperidine-1-carboxylateHCID 22266191—

Reaction Steps

t-Butyl (1-t-butoxycarbonylpiperidin-4-yl)phenylcarbamate (290 mg) was dissolved in trifluoroacetic acid-dichloromethane (10%, 20 mL) and stirred at room temperature for 2 h. The solvent was evaporated under reduced pressure and the residue was partitioned between aqueous sodium hydroxide (2M) and ether (30 mL). The organic layer was separated, dried (MgSO4) and the solvent was evaporated under reduced pressure. The residue was dissolved in dichloromethane (20 mL) and cooled in ice. Di-t-butyldicarbonate (161 mg) was added and the mixture was stirred at room temperature for 30 min. The solvent was evaporated under reduced pressure and the residue was purified by MPLC on silica gel, eluting with EtOAc/Hexane (5:95) to give the title compound as a clear oil (141 mg), δH (CDCl3) 1.55 (9H, s), 1.59 (2H, m), 1.82 (2H, m), 2.58 (1H, m), 2.77 (1H, m), 3.64 (2H, br s), 4.16 (2H, m), 6.68-6.79 (2H, m), 7.01-7.26 (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05885999
Source datasetuspto-grants-1999_03
ORD IDord-440995c7154948ddb8398d636b6b85b8
Source noteuspto-grants-1999_03