HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 251990Generated: October 29, 2026
Acetic Anhydride → 2-Acetamido-3-methylbenzoic acid
https://huagongshe.com/reaction/251990
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2-Amino-3-methylbenzoic acid | HCID 78101 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Acetamido-3-methylbenzoic acid | HCID 12639204 | 38% |
Reaction Steps
A mixture of 1.51 g of 2-amino-3-methylbenzoic acid, 1.0 g of acetic anhydride and 20 ml of tetrahydrofuran was stirred at 80° C. for 13 hours. The reaction mixture was allowed to cool to room temperature, poured into water, and extracted with ethyl acetate two times. The organic layers were combined, washed successively with water and an aqueous saturated sodium chloride solution, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The resulting residue was washed with ethyl acetate to obtain 0.72 g of 2-acetylamino-3-methylbenzoic acid of the formula:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07867949B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-124e0681d35a4289998bafbdc3cb2551 |
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| Source note | uspto-grants-2011_01 |
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