Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 279312Generated: October 26, 2026

Ether hydrochloride → 4-[{N-(3(trifluoromethyl)benzoyl)glycyl}aminomethyl]piperidine

https://huagongshe.com/reaction/279312

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEther hydrochlorideHCID 10953452—
Reactant1-(tert-butoxycarbonyl)-4-[[N-(3-(trifluoromethyl)benzoyl)glycyl]aminomethyl]piperidineHCID 18426150—
SolventMethanolHCID 887—
Product4-[{N-(3(trifluoromethyl)benzoyl)glycyl}aminomethyl]piperidineHCID 1842616472%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 1-(tert-butoxycarbonyl)-4-[{N-(3-(trifluoromethyl)benzoyl)glycyl}aminomethyl]piperidine (2.29 g, 5.16 mmol) in CH3OH (40 mL) was treated with 1 N HCl-Et2O (55 mL). The reaction mixture was stirred at 25° C. for 15 h and the solvent was removed under reduced pressure. 2 N aqueous NaOH solution (100 mL) was added to the reaction mixture and the mixture was extracted with EtOAc (3×100 mL). The combined extracts were washed with brine and dried (K2CO3). The solvent was removed under reduced pressure to afford a white solid which was purified by column chromatography (SiO2, CH3OH/CH2Cl2/Et3N=7/6/1)) to give 4-[{N-(3-(trifluoromethyl)benzoyl)glycyl}aminomethyl]piperidine as a white solid (1.27 g, 72%): The purity was determined by RPLC/MS (98%); ESI/MS m/e 344.1 (M++H, C16H20F3N3O2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06362177B1
Source datasetuspto-grants-2002_03
ORD IDord-a8b2e11a92cf4123a135cb71336a01a9
Source noteuspto-grants-2002_03