HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → n-(5-methoxy-2-methylphenyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-Methoxy-o-toluidine | HCID 99500 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | n-(5-methoxy-2-methylphenyl)acetamide | HCID 231720 | — |
Reaction Steps
To a solution of triethylamine (2.9 g, 14.4 mmol) and 5-methoxy-2-methylaniline (1.0 g, 7.2 mmol) in DCM (30 mL) at 0° C., was added acetyl chloride (0.57 g, 7.2 mmol) dropwise. The mixture was stirred at room temperature for 1 hour. The reaction was quenched with saturated ammonium chloride aqueous solution, and extracted with DCM. The organic layer was dried over Na2SO4 and concentrated to give N-(5-methoxy-2-methylphenyl)acetamide as needle-shaped crystals. The crude product was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08859574B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-627d8e40b7c5452380667d70523e8c98 |
| Source note | uspto-grants-2014_10 |