HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042730Generated: October 27, 2026
Triethylamine → 3-bromo-4-fluoro-N-(2-fluoro-3-(trifluoromethyl)phenyl)benzamide
https://huagongshe.com/reaction/1042730
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Bromo-4-fluorobenzoyl chloride | HCID 69598 | — |
| Reactant | 3-Amino-2-fluorobenzotrifluoride | HCID 145569 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-bromo-4-fluoro-N-(2-fluoro-3-(trifluoromethyl)phenyl)benzamide | HCID 59427998 | — |
Reaction Steps
2-Fluoro-3-(trifluromethyl)aniline (0.515 g, 0.37 mL, 2.88 mmol) was added to a solution of 3-bromo-4-fluorobenzoyl chloride (0.650 g, 2.74 mmol) in dichloromethane (5 ml), and the mixture stirred at room temperature for 30 min. Triethylamine (0.360 g, 0.50 ml, 3.56 mmol) was added and the solution stirred at room temperature for 1 h. The reaction mixture was partitioned between dichloromethane and saturated aqueous sodium bicarbonate solution. The aqueous phase was separated and extracted with dichloromethane. The combined organic phases were washed with water, brine, dried over anhydrous sodium sulfate, filtered, and concentrated to afford a light yellow solid. Trituration with dichloromethane and filtering afforded 3-bromo-4-fluoro-N-(2-fluoro-3-(trifluoromethyl)phenyl)benzamide as a white solid. MS (M−H+) 377.9; Calculated for C14H7BrF5NO: 379.
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-65ca380cbc5240f69c22d949f24214c8 |
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| Source note | uspto-grants-2013_10 |
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