HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 57467435, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | 2-Methyl-2-phenoxypropanamide | HCID 12321512 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57467435 | HCID 57467435 | — |
Reaction Steps
To a solution of 2-methyl-2-phenoxypropanamide from Step C (0.01 mol) in dry CH2Cl2 (50 mL) and triethylamine (3.03 g, 0.03 mol) at 0° C. was added trifluoroacetic anhydride (3.15 g, 0.015 mol). After the addition was complete, the solution was allowed to warm to room temperature and stirring was continued at ambient temperature overnight. The reaction mixture was then refluxed for 3 hours. After cooling to room temperature and dilution with CH2Cl2 (100 mL), the solution was washed with saturated aqueous NaHCO3 (50 mL×3), water, and brine and dried over sodium sulfated. Evaporation gave the titled compound. 1H NMR (400 MHz, CDCl3) δ ppm 7.32˜7.36 (m, 2H), 7.14˜7.20 (m, 3H), 1.71 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08507493B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-d06c4abb71ac42d49bfeee6ffa365b06 |
| Source note | uspto-grants-2013_08 |