Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1667070Generated: October 25, 2026

4-(Trifluoromethyl)benzylamine → 2-(2-oxo-3,3-diphenylpyrrolidin-1-yl)-N-[4-(trifluoromethyl)benzyl]acetamide

https://huagongshe.com/reaction/1667070

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethyl)benzylamineHCID 76804—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant2-(2-Oxo-3,3-diphenylpyrrolidin-1-yl)acetic acidHCID 67359013—
SolventDichloromethaneHCID 6344—
Product2-(2-oxo-3,3-diphenylpyrrolidin-1-yl)-N-[4-(trifluoromethyl)benzyl]acetamideHCID 45275598—

Reaction Steps

A solution of (4-(trifluoromethyl)phenyl)methanamine (0.033 g, 0.186 mmol), 2-(2-oxo-3,3-diphenylpyrrolidin-1-yl)acetic acid (Example 1C, 0.050 g, 0.169 mmol) and N1-((ethylimino)methylene)-N3,N3-dimethylpropane-1,3-diamine hydrochloride (0.049 g, 0.254 mmol) in dichloromethane (0.5 mL) was stirred at room temperature. After stirring overnight, the reaction was loaded directly onto a SF15-12 column (Analogix®, Burlington, Wis.), and the title compound was eluted using a gradient of 5% to 100% ethyl acetate/hexanes over 20 minutes (flow=30 mL/minute). 1H NMR (300 MHz, CDCl3) δ ppm 7.50-7.54 (m, 2H), 7.17-7.33 (m, 12H), 6.39 (t, J=6.1 Hz, 1H), 4.34 (d, J=6.1 Hz, 2H), 4.07 (s, 2H), 3.51 (t, J=6.5 Hz, 2H), 2.81 (t, J=6.5 Hz, 2H); MS (ESI−) m/z 451 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044069B2
Source datasetuspto-grants-2011_10
ORD IDord-af68d0625ebd443c99186b944eb6ee24
Source noteuspto-grants-2011_10