HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → N-(2-Bromo-5-chloro-4-methoxyphenyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-Bromo-5-chloro-4-methoxybenzenamine | HCID 45156706 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(2-Bromo-5-chloro-4-methoxyphenyl)acetamide | HCID 68535198 | 69.4% |
Reaction Steps
4.40 g (18.6 mmol) 2-Bromo-5-chloro-4-methoxy-aniline and 3.1 ml (22.0 mmol) triethylamine were dissolved in 50 ml THF. 1.42 ml (20.0 mmol) acetylchloride were added dropwise at room temperature. The reaction mixture was stirred at room temperature for additional 2 hours, saturated NaHCO3 solution was added and the mixture was extracted with ethyl acetate. Removal of the solvent and crystallisation with ether gave 3.6 g (12.9 mmol, 69%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07645760B2 |
| Source dataset | uspto-grants-2010_01 |
| ORD ID | ord-7277291a1405423487eb8888b8c9f8f1 |
| Source note | uspto-grants-2010_01 |