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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-Morpholinoethylamine | HCID 408285 | — |
| Reactant | 3-Nitro-5-(trifluoromethyl)benzoic acid | HCID 616602 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(2-morpholinoethyl)-3-nitro-5-(trifluoromethyl)benzamide | HCID 59427894 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08557996B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-54353f93d0ec4396857d069c8f3baff7 |
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| Source note | uspto-grants-2013_10 |
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