HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → N-[4-Bromo-2-fluoro-5-(trifluoromethyl)phenyl]acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 4-Bromo-2-fluoro-5-(trifluoromethyl)aniline | HCID 7018046 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | N-[4-Bromo-2-fluoro-5-(trifluoromethyl)phenyl]acetamide | HCID 23274446 | 83% |
Reaction Steps
A mixture of compound 22 (3.6 g, 14 mmol), acetic anhydride (8 mL) and pyridine (0.1 mL) was stirred at room temperature for 1 h, then concentrated in vacuo. The residue was added ice and sodium bicarbonate (until pH=7). The resulted mixture was extracted with EtOAc. The organic layers were combined, washed by brine, dried over Na2SO4, filtered and concentrated to give the title compound 23 (3.5 g, 83%). 1H NMR (400 MHz, CDCl3) δ8.79 (d, 1H, J=7.8 Hz), 7.46 (d, 1H, J=10.0 Hz), 7.38 (br s, 1H), 2.24 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09216957B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-2db1ba29aff14a2cbaa47ab2a7b3323c |
| Source note | uspto-grants-2015_12 |