HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → N-(2-Bromo-4-isopropylphenyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Bromo-4-isopropylaniline | HCID 521337 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(2-Bromo-4-isopropylphenyl)acetamide | HCID 258023 | 96.8% |
Reaction Steps
A mixture of 2-bromo-4-isopropylaniline (5.05 g, 23.6 mmol), acetic anhydride (2.4 mL, 25 mmol), and triethylamine (3.5 mL, 25 mmol) in dichloromethane (25 mL) was stirred at ambient temperature for 4 days. The mixture was diluted with dichloromethane, washed sequentially with saturated aqueous Na2CO3 and 1M HCl, dried (MgSO4), filtered, and concentrated to provide the desired product (5.85 g). MS (DCI) m/e 256, 258 (M+H)+; 273, 275 (M+NH4)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07491718B2 |
| Source dataset | uspto-grants-2009_02 |
| ORD ID | ord-4231c22b169e4caf978815a54b69cbe5 |
| Source note | uspto-grants-2009_02 |