HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 130327Generated: October 30, 2026
Water → 5,7-Dimethoxy-2-methyl-4H-benzo[d][1,3]oxazin-4-one
https://huagongshe.com/reaction/130327
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Amino-4,6-dimethoxybenzoic acid | HCID 11658456 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5,7-Dimethoxy-2-methyl-4H-benzo[d][1,3]oxazin-4-one | HCID 11506814 | 51% |
Reaction Steps
The anthranilic acid (388 mg, 1.97 mmol) prepared in Example 2 was taken up in anhydrous methylene chloride (10 mL). Triethylamine (2.36 mmol) was added followed by addition of acetic anhydride (2.36 mmol). The reaction mixture was heated at 40° C. for 18 hours. Subsequently, the reaction mixture was poured into water and extracted with methylene chloride. The organic layer was washed with saturated aqueous sodium bicarbonate, brine, dried over magnesium sulfate, filtered, and concentrated in vacuo to afford 5,7-dimethoxy-2-methyl-3,1-benzoxazine-4-one (51% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07381730B2 |
|---|
| Source dataset | uspto-grants-2008_06 |
|---|
| ORD ID | ord-1ebffd0b0898464cab00db3f99018f95 |
|---|
| Source note | uspto-grants-2008_06 |
|---|