HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247213Generated: October 29, 2026
Acetyl chloride → N-(2-Bromo-5-nitrophenyl)acetamide
https://huagongshe.com/reaction/2247213
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Bromo-5-nitroaniline | HCID 82607 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(2-Bromo-5-nitrophenyl)acetamide | HCID 21959509 | — |
Reaction Steps
2-Bromo-5-nitroaniline (10 g) was dissolved in CH2Cl2 (500 mL), DIEA (6.6 g) was added to the mixture, followed by 100 mg of DMAP. The mixture was cooled to 0° C. in ice bath. Acetyl chloride (4 g in 50 mL CH2Cl2) was added dropwise to the reaction mixture. After the mixture was stirred at RT over 3 h, and extracted once with saturated NaHCO3 solution and once with brine. The resulting organic layer was dried over MgSO4, filtered and concentrated in vacuo. The crude material was purified by flash chromatography on silica gel with 1:1 EtOAc:Hexane to 100% EtOAc to afford a white solid. MS: 258 (M−1). Calc'd. for C8H7BrN2O3—259.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07687643B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-09895d0522de4dcba593bbaf38c2ddea |
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| Source note | uspto-grants-2010_03 |
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