HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554133Generated: October 27, 2026
Ethylmorpholine → 2-Chloro-4-fluoro-3-(trifluoromethyl)benzamide
https://huagongshe.com/reaction/554133
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylmorpholine | HCID 7525 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | ammonium 1H-1,2,3-benzotriazol-1-olate | HCID 23118068 | — |
| Reactant | 2-Chloro-4-fluoro-3-(trifluoromethyl)benzoic acid | HCID 67460618 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Chloro-4-fluoro-3-(trifluoromethyl)benzamide | HCID 67460657 | 88.3% |
Reaction Steps
2-Chloro-4-fluoro-3-(trifluoromethyl)benzoic acid (0.560 g, 2.31 mmol), ammonium 1H-1,2,3-benzotriazol-1-olate (0.534 g, 3.47 mmol, prepared as described below), N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (0.643 g, 3.47 mmol), and N-ethyl morpholine (0.594 ml, 4.62 mmol) were stirred together in dichloromethane (30 ml) for a total of 3 hrs. Saturated aqueous sodium hydrogen carbonate (30 ml) was added and the mixture was stirred for 15 minutes. The organic layer was separated using a hydrophobic frit and then washed with 2N aqueous hydrogen chloride (2×50 ml). Separation of the organic layer, again using a hydrophobic frit, and evaporation in vacuo gave 2-chloro-4-fluoro-3-(trifluoromethyl)benzamide (0.493 g) as an off-white solid which was used without further purification in the subsequent step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08048907B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-26c7661f20e14df1a534bc52edccf8f1 |
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| Source note | uspto-grants-2011_11 |
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