HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → N-[7-(Trifluoromethyl)-2-naphthalenyl]acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 7-(Trifluoromethyl)naphthalen-2-amine | HCID 18451539 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[7-(Trifluoromethyl)-2-naphthalenyl]acetamide | HCID 18451538 | — |
Reaction Steps
To a solution of 7-trifluoromethyl-2-aminonaphthalene (550 mg, 2.60 mmol) and triethylamine (1.09 mL, 7.81 mmol) in dichloromethane (10 mL) at room temperature is added acetyl chloride (0.222 mL, 3.13 mmol) dropwise. After stirring at room temperature for 1.5 hours, the mixture is partitioned between dichloromethane and water. The organic layer is washed with 0.1 M citric acid solution, brine, dried (MgSO4) and concentrated by rotary evaporator to give 7-trifluoromethyl-2-acetamidonaphthalene as a light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07202364B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-d8eb814c16ab403ca891abc81650745b |
| Source note | uspto-grants-2007_04 |