HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-Bromo-N-methyl-N-[(4-nitrophenyl)methyl]acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Reactant | N-methyl-1-(4-nitrophenyl)methanamine | HCID 409440 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 2-Bromo-N-methyl-N-[(4-nitrophenyl)methyl]acetamide | HCID 19974447 | 104.6% |
Reaction Steps
To a solution of bromoacetyl bromide (30 g) in methylene chloride (20 ml) at 0° was added a solution of N-methyl-4-nitrobenzenemethanamine (8.3 g; G. I. Wilson, J. Chem. Soc., 1926, 2461) in methylene chloride (10 ml) and triethylamine (12 ml). The reaction was stirred 5 min. at 0° and then water (20 ml) was added. The methylene chloride layer was dried and evaporated in vacuo. The residue was purified by column chromatography eluting with methylene chloride/methanol (97:3) to give the title compound (15 g) as an oil. NMR includes signals at d 3.1(3H,s,N--CH3); 3.9(2H,s,CH2Br); 4.55(2H,s,Ph--CH2 --N); 7.0-8.3(4H,m,aromatics).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05604237 |
| Source dataset | uspto-grants-1997_02 |
| ORD ID | ord-1a67e430599c4101b9bb2072d5efaa11 |
| Source note | uspto-grants-1997_02 |