HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 178526759, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | 5-Bromo-2-(2-nitrovinylamino)benzoic acid | HCID 53405055 | — |
| Product | HCID 178526759 | HCID 178526759 | — |
Reaction Steps
5-Bromo-2-(2-nitrovinylamino)benzoic acid (Compound of step 1, 25 g, 87 mmol) and potassium acetate (10.5 g, 104 mmol) in acetic anhydride (112 mL, 1185 mmol) were stirred for 3 hours at 120° C. The precipitate was filtered, and washed with acetic acid till the filtrate was colorless. It was further washed with water and dried to obtain the title compound. Yield: 15 g (64%); 1H NMR (CDCl3, 500 MHz): δ 9.275 (s, 1H), 8.611-8.615 (d, 1H, J=2 Hz), 8.100-8.118 (d, 1H, J=9 Hz), 8.026-8.048 (dd, 1H, J=8.5 Hz, 2 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08637670B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-e6f84824a38a418d8be2ef1c97c2e206 |
| Source note | uspto-grants-2014_01 |