HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2107004Generated: October 30, 2026
5-Aminosalicylic Acid → N-Acetyl-5-Aminosalicylic Acid
https://huagongshe.com/reaction/2107004
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-Aminosalicylic Acid | HCID 4075 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-Acetyl-5-Aminosalicylic Acid | HCID 65512 | 67% |
Reaction Steps
2-Hydroxy-5-aminobenzoic acid (20.0 g, 0.131 mole) was suspended in water (100 ml), and acetic anhydride (15.0 ml) was added. The reaction mixture was heated to 100° C., with stirring, for 10 minutes, cooled in an ice bath, and the product was isolated by filtration. After recrystallization from water, with activated carbon, analytically pure 2-hydroxy-5-acetamidobenzoic acid (17.0 g, 67%) was obtained, m.p. 218°-220° C. Found (Calc. for C9H9NO4) C 55.10 (55.38), H 4.61 (4.62), N 7.10 (7.18).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04933330 |
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| Source dataset | uspto-grants-1990_06 |
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| ORD ID | ord-ef8be6134b0148d396fac84d94b80cf8 |
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| Source note | uspto-grants-1990_06 |
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