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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348120Generated: October 30, 2026

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

https://huagongshe.com/reaction/348120

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
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 numberUS07176196B2
Source datasetuspto-grants-2007_02
ORD IDord-00bd981a0c2447ff9afadabca3988d5e
Source noteuspto-grants-2007_02