HuagongsheHuagongshe Chemistry Print Report · For research reference only
m-Toluidine → 2-bromo-N-(3-methylphenyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | m-Toluidine | HCID 7934 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Bromoacetyl chloride | HCID 89602 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-bromo-N-(3-methylphenyl)acetamide | HCID 225528 | — |
Reaction Steps
To a slurry of m-toluidine (15.5 mL, 140 mmol) in a 2N aqueous solution of sodium hydroxide (75 mL) was added dropwise a solution of bromoacetyl chloride (11.6 mL, 140 mmol) in dichloromethane (50 mL) and the reaction mixture was stirred at room temperature for about 30 min. The layers were separated and the organic layer was washed with 1N aqueous hydrochloric acid, dried (MgSO4), filtered and concentrated under vacuum. The residue was triturated twice from dichloromethane/hexane (1:4) to provide 2-bromo-N-m-tolyl-acetamide. MS (DCI-NH3): m/z 245, 247 (M+NH3)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07468371B2 |
| Source dataset | uspto-grants-2008_12 |
| ORD ID | ord-d48ea276fc0c4cb981733fa548f4f2ad |
| Source note | uspto-grants-2008_12 |