HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 992491Generated: October 26, 2026
Acetic Acid → 3-Acetamido-4-nitrophthalic anhydride
https://huagongshe.com/reaction/992491
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2,3-Dimethyl-6-nitroaniline | HCID 597166 | — |
| Product | 3-Acetamido-4-nitrophthalic anhydride | HCID 15511835 | — |
Reaction Steps
2,3-Dimethyl-6-nitroaniline was acetylated in acetic acid by using 1 equivalence of acetic anhydride, and the product was recrystallized from ethanol. The resulting 3-acetamido-4-nitroxylene was dissolved in boiled water containing magnesium sulfate. To the solution, 6 equivalences of potassium permanganate suspended in water was added in several portions, and the solution was refluxed until purple color disappeared. The hot reaction mixture was filtered and cooled, and then the filtrate was made acidic with hydrochloric acid and extracted with ethyl acetate. The resulting 3-acetamido-4-nitrophthalic acid was dehydrated in acetic anhydride using acetyl chloride. The reaction mixture was concentrated under reduced pressure, and then a small quantity of anhydrous methylene chloride was added to the residue and the deposited solid was collected by filtration to obtain 3-acetamido-4-nitrophthalic anhydride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06469051B2 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-5de86976a84143a5aaa16afadef8343d |
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| Source note | uspto-grants-2002_10 |
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