HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 4-Nitrophthalic acid anhydride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 1,2-Benzenedicarboxylic acid, 4-nitro- | HCID 69121 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-Nitrophthalic acid anhydride | HCID 230976 | — |
Reaction Steps
A mixture of 21.1 g of 4-nitrophthalic acid and 50.0 g of acetic anhydride were heated at reflux for 6 hours, following which the acetic acid was removed by distillation at atmospheric pressure. The excess acetic anhydride was removed by distillation at 15 mm Hg pressure with the flask temperature not exceeding 120° C, leaving a quantitative yield of crude 4-nitrophthalic anhydride, m.p. 114°-116° C. The product was recrystallized from chloroform to afford a 93% yield of product, m.p. 123°-124° C, identical to that of Example 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04131730 |
| Source dataset | uspto-grants-1978_12 |
| ORD ID | ord-acba7cf0bb274137aa2ea882011060e1 |
| Source note | uspto-grants-1978_12 |