HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → N-[4-chloro-2-(trifluoromethyl)phenyl]acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Benzenamine, 4-chloro-2-(trifluoromethyl)- | HCID 67961 | — |
| Product | N-[4-chloro-2-(trifluoromethyl)phenyl]acetamide | HCID 6461606 | 91.7% |
Reaction Steps
A solution of 2-amino-5-chlorobenzotrifluoride (1.01 g, 5.16 mmol, Aldrich) in acetic anhydride (5 mL) was stirred at room temperature for 12 h to produce white needle precipitate. It was filtered to give 1.123 g (91.7%) of 2-acetamido-5-chlorobenzotrifluoride. 1H NMR (CDCl3): δ 2.214 (S, 3H); 7.359 (br, 1H); 7.512 (d, 1H, J=9 Hz), 7.581 (s, 1H); 7.163 (d, 1H, J=8.4 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05620979 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-45fe24d03aa047729048bcccdf28bb0c |
| Source note | uspto-grants-1997_04 |