HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 557359Generated: October 29, 2026
Acetyl chloride → N-(2-Bromo-5-nitrophenyl)acetamide
https://huagongshe.com/reaction/557359
Participants
| Role | Name | HCID | Charge |
|---|
| 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 500 mL of CH2Cl2, DIEA (6.6 g) was added to the mixture, followed by DMAP (100 mg). 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, 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 N-(2-bromo-5-nitrophenyl)acetamide as a white solid. MS: 258 (M−1). Calc'd. for C8H7BrN2O3−259.06.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08058445B2 |
|---|
| Source dataset | uspto-grants-2011_11 |
|---|
| ORD ID | ord-31f51a1772db4c7e92ef8d1226fd7e7e |
|---|
| Source note | uspto-grants-2011_11 |
|---|