HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1830992Generated: October 25, 2026
2-Nitrobenzoyl chloride → N-[4-bromo-3-(trifluoromethyl)phenyl]-2-nitrobenzamide
https://huagongshe.com/reaction/1830992
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Nitrobenzoyl chloride | HCID 11875 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Bromo-3-(trifluoromethyl)aniline | HCID 67852 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-[4-bromo-3-(trifluoromethyl)phenyl]-2-nitrobenzamide | HCID 1300995 | — |
Reaction Steps
A solution of 3-amino-6-bromobenzotrifluoride (Fluka, Buchs, Switzerland; 24.0 g, 100 mmol) in EtOAc (240 mL) is added to a stirred aqueous solution of sodium hydroxide (110 mL of 1 M) at room temperature. This stirred solution is then treated dropwise over 30 minutes with a solution of 2-nitrobenzoyl chloride (Fluka, Buchs, Switzerland; 14.5 mL, 110 mmol) in EtOAc (150 mL). The resulting mixture is then stirred for 30 min at ambient temperature. The mixture is extracted with EtOAc (3×100 mL) and the combined extracts are sequentially washed with hydrochloric acid (2×100 mL of 2M), water (2×100 mL), saturated aqueous sodium hydrogen carbonate solution (2×100 mL) and saturated aqueous sodium chloride (1×100 mL), dried (MgSO4), filtered and the solvent is evaporated under reduced pressure to yield the crude product which is purified by recrystallisation from EtOAc-hexane to give the title compound as a beige crystalline solid, m.p. 157–158° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07067543B2 |
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| Source dataset | uspto-grants-2006_06 |
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| ORD ID | ord-fc201deeec7d410ea7b4430c763c67dc |
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| Source note | uspto-grants-2006_06 |
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