HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 843978Generated: October 30, 2026
Bromine → N-(2-Bromophenyl)-2,2,2-trifluoroacetamide
https://huagongshe.com/reaction/843978
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromine | HCID 24408 | — |
| Reactant | 2,2,2-Trifluoro-N-phenylacetamide | HCID 67881 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-(2-Bromophenyl)-2,2,2-trifluoroacetamide | HCID 4263215 | — |
Reaction Steps
To a stirred mixture of the N-trifluoroacetylaniline (2.00 mmol) and sodium hydrogen carbonate (0.21 g, 2.50 mmol, 1.25 eq) in methanol (10 mL) at 0° C. is added dropwise bromine (0.113 mL, 2.19 mmol, 1.1 eq). The resulting reaction mixture is then stirred at 25° C. for 30 minutes. The reaction mixture is then evaporated under reduced pressure, and the residue is placed in water made acidic to pH 3 with HCl (10 mL). This aqueous mixture is extracted with ethyl acetate (3×15 mL). The extracts is combined, dried (MgSO4), and evaporated under reduced pressure. The residue is column chromatographed using silica gel (approximately 50 g) and elution with an appropriate solvent system to afford the corresponding 2-bromo-N-trifluoroacetylaniline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06380233B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-54c7d2970c01459db69074daf15ff12e |
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| Source note | uspto-grants-2002_04 |
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