HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → N-(4-bromo-3,5-dimethylphenyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 4-Bromo-3,5-dimethylaniline | HCID 12383117 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(4-bromo-3,5-dimethylphenyl)acetamide | HCID 4246250 | — |
Reaction Steps
To a solution of 4-bromo-3,5-dimethyl-phenylamine (130 mg) in CH2Cl2 (4 mL) was added acetic anhydride (0.123 mL) at 0° C. The mixture was allowed to warm up to room temperature and stirred for 2 h. The mixture was concentrated under reduced pressure. The crude product was purified by column chromatography (SiO2, EtOAc:Hexane=10:90 to 60:40) to give N-(4-bromo-3,5-dimethyl-phenyl)-acetamide: MS (m/z) 244 (M+1); 1H NMR (CDCl3, 400 MHz) δ 7.24 (s, 2H), 2.35 (s, 6H), 2.13 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08222248B2 |
| Source dataset | uspto-grants-2012_07 |
| ORD ID | ord-f20b2d39806543dd80d8ee31b0c9053e |
| Source note | uspto-grants-2012_07 |