HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → N-(2-tert-butylphenyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-tert-Butylaniline | HCID 80574 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(2-tert-butylphenyl)acetamide | HCID 343805 | 95.7% |
Reaction Steps
To a solution of 2-tert-butylaniline (5.0 g, 33.5 mmol) and triethylamine (11.2 g, 110.6 mmol) in THF (350 mL) was added acetyl chloride (2.89 g, 36.9 mmol). After being stirred at room temperature for 3 h, the reaction mixture was partitioned between ethyl acetate and water. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The resulting white solid was triturated with hexane/ethyl acetate to give the title compound (6.13 g) as a white crystalline powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08853215B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-caa101ae1e0b48a99cf2072b2995831c |
| Source note | uspto-grants-2014_10 |