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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1664120Generated: November 2, 2026

Trifluoroacetic acid → 2-(Aminomethyl)-5-fluoro-n-methylbenzamide trifluoroacetate salt

https://huagongshe.com/reaction/1664120

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant2-Bromo-5-fluorobenzoic acidHCID 2778181—
ReactantTert-butyl 4-fluoro-2-[(methylamino)carbonyl]benzylcarbamateHCID 11984298—
SolventDichloromethaneHCID 6344—
Product2-(Aminomethyl)-5-fluoro-n-methylbenzamide trifluoroacetate saltHCID 2106981499%

Reaction Steps

To a solution of tert-butyl 4-fluoro-2-(methylcarbamoyl)benzylcarbamate (7.70 g, 27.3 mmol), prepared from 2-bromo-5-fluorobenzoic acid using literature methods in CH2Cl2 (100 mL) was added CF3CO2H (25 mL) and the mixture stirred at room temperature for 15 min. This was concentrated in vacuo and the residue triturated with diethyl ether to obtain 8.0 g (Yield 99%) of the title compound as a white powder. 1H NMR (300 MHz, D2O) δ ppm: 2.93 (3H, s) 4.20 (2H, s) 7.35 (1H, dt, J=8.5, 3 Hz) 7.42 (1H, dd, J=9.0, 2.7 Hz) 7.57 (1H, dd, J=8.4, 5.5 Hz); LC/MS m/z 183 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039458B2
Source datasetuspto-grants-2011_10
ORD IDord-7e98c8eae9884b3f8eef1cb5c6c51529
Source noteuspto-grants-2011_10