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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
Reactant2-Amino-4,6-dimethoxybenzoic acidHCID 11658456—
SolventDichloromethaneHCID 6344—
Product5,7-Dimethoxy-2-methyl-4H-benzo[d][1,3]oxazin-4-oneHCID 1150681451%

Reaction Conditions

Temperature40 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07381730B2
Source datasetuspto-grants-2008_06
ORD IDord-1ebffd0b0898464cab00db3f99018f95
Source noteuspto-grants-2008_06