HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetamide, N-(3,5-dimethylphenyl)- → N-(4-bromo-3,5-dimethylphenyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetamide, N-(3,5-dimethylphenyl)- | HCID 74903 | — |
| Reactant | Benzyltrimethylammoniumtribromide | HCID 53442637 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Product | N-(4-bromo-3,5-dimethylphenyl)acetamide | HCID 4246250 | 90% |
Reaction Steps
Benzyltrimethylammonium tribromide (BTMA-Br3) (7.8 g, 20.21 mmol) was added to a solution of N-(3,5-dimethyl-phenyl)-acetamide (3.0 g, 18.38 mmol) in CH2Cl2/MeOH (90 ml/90 ml) at room temperature in an Ar atmosphere. The reaction mixture was stirred at room temperature for 10 minutes. The reaction mixture was concentrated under reduced pressure, and CH2Cl2 was then added to the resulting residue. The organic layer was washed with H2O, and then dried over anhydrous Na2SO4 and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:EtOAc=1:1) to give N-(4-bromo-3,5-dimethyl-phenyl)-acetamide (4.0 g, yield 90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09169254B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-377a7f6a6e6547a096434dc56397f3d7 |
| Source note | uspto-grants-2015_10 |