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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042690Generated: October 26, 2026

Triethylamine → N-(2-morpholinoethyl)-3-nitro-5-(trifluoromethyl)benzamide

https://huagongshe.com/reaction/1042690

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantThionyl ChlorideHCID 24386—
Reactant2-MorpholinoethylamineHCID 408285—
Reactant3-Nitro-5-(trifluoromethyl)benzoic acidHCID 616602—
SolventDichloromethaneHCID 6344—
ProductN-(2-morpholinoethyl)-3-nitro-5-(trifluoromethyl)benzamideHCID 59427894—

Reaction Conditions

Temperature75 °C

Reaction Steps

A mixture of 3-nitro-5-(trifluoromethyl)benzoic acid (300 mg, 1.29 mmol, 1.0 equiv) and thionyl chloride (2.0 ml) was heated at 75° C. for 1 h. The solvent was removed in vacuo and the residue taken up in CH2Cl2 (5.0 ml). To the solution was added 2-morpholinoethanamine (185 mg, 1.42 mmol, 1.1 equiv) and triethylamine (0.54 ml, 3.86 mmol, 3.0 equiv). After the reaction was complete, the solution was diluted with CH2Cl2 (ca.10 ml) and washed with water and brine. After drying with Na2SO4 and concentration in vacuo, the resulting N-(2-morpholinoethyl)-3-nitro-5-(trifluoromethyl)benzamide was advanced without further purification. MS m/z: 348 (M+H+); Calculated for C14H16F3N3O4: 347.1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557996B2
Source datasetuspto-grants-2013_10
ORD IDord-54353f93d0ec4396857d069c8f3baff7
Source noteuspto-grants-2013_10