HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1692184Generated: November 2, 2026
Acetic Acid → 2-Amino-5-Chloro-N,3-Dimethylbenzamide
https://huagongshe.com/reaction/1692184
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 5-Chloro-3-methyl isatoic anhydride | HCID 11550259 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Amino-5-Chloro-N,3-Dimethylbenzamide | HCID 25068251 | 94% |
Reaction Steps
A 250-mL flask equipped with thermometer and nitrogen bubbler was charged with 6-chloro-8-methyl-2H-3,1-benzoxazine-2,4(1H)-dione (21.0 g, 0.099 mol) (i.e. the product of Example 1), ethyl acetate (100 mL), and acetic acid (12.6 g, 0.21 mol). The mixture was stirred at 22° C., and anhydrous methylamine (4.3 g, 0.14 mol) was added below the surface of the mixture in portions over 45 minutes while maintaining the temperature at 22-41° C. The mixture was held for 2 h at 40° C., then water (150 mL) was added, and the ethyl acetate was removed by distillation. When the pot temperature reached 83° C., the solution was seeded, and the product slurry was cooled over about 2 h to 10° C. The solid was collected by filtration, washed with water and dried to afford the title compound as a white crystalline solid (18.38 g, >97.4 wt. % purity by HPLC, 94% yield) melting at 143-145° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08153844B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-f99c68e3cd58494ea85d2348797c8862 |
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| Source note | uspto-grants-2012_04 |
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