HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 4-(Acetyloxy)-3-nitrobenzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 4-Hydroxy-3-nitrobenzoic acid | HCID 12033 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 4-(Acetyloxy)-3-nitrobenzoic acid | HCID 14057307 | — |
Reaction Steps
To 4-hydroxy-3-nitrobenzoic acid (10 g) were added pyridine (12 ml) and acetic anhydride (55 ml), and the mixture was stirred at room temperature for 65 hours. The reaction solution was concentrated under reduced pressure, and thereto was added a 5% aqueous sodium hydrogen sulfate solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with a saturated aqueous sodium chloride solution, dried over sodium sulfate, filtered and concentrated under reduced pressure to give the title compound (11.7 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08389511B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-08f9aeba1a974cd8b246e3d336654e04 |
| Source note | uspto-grants-2013_03 |