Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045942Generated: October 31, 2026

Phosgene → 5-Methoxy-2H-3,1-benzoxazine-2,4(1H)-dione

https://huagongshe.com/reaction/1045942

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosgeneHCID 6371—
ReactantSodium HydroxideHCID 14798—
Reactant2-Amino-6-methoxybenzoic AcidHCID 2735357—
SolventWaterHCID 962—
Product5-Methoxy-2H-3,1-benzoxazine-2,4(1H)-dioneHCID 1075029565.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

Phosgene (4.72 ml, 8.97 mmol; 20% in toluene) was added dropwise to a solution of 2-amino-6-methoxybenzoic acid (1 g, 5.98 mmol) in 2N aqueous sodium hydroxide (6.28 ml, 12.56 mmol) and water (15 ml) cooled to 0° C. over a period of 15 minutes, maintaining the temperature at 0-5° C. The resulting suspension was stirred at 0° C. for 15 minutes. The precipitate was collected by filtration, washed with water, followed by a small amount of acetonitrile and ether and dried under vacuum at 40° C. to afford 5-methoxy-1H-3,1-benzoxazine-2,4-dione (0.760 g, 65.8%) as a beige solid. 40% aqueous methylamine (1.57 ml, 18.1 mmol) was added to a stirred suspension of 5-methoxy-1H-3,1-benzoxazine-2,4-dione (700 mg, 3.62 mmol;) in water (5 ml). The resulting solution was stirred at room temperature for 36 hours. The mixture was diluted with EtOAc, washed sequentially with saturated aqueous sodium carbonate, water and brine. The organic layer was dried over MgSO4 and evaporated to afford 2-amino-6-methoxy-N-methylbenzamide (457 mg, 70.0%) as a white solid. 1H NMR spectrum (500 MHz, DMSO): 2.73 (d, 3H), 3.73 (s, 3H), 5.79 (bs, 2H), 6.19 (d, 1H), 6.30 (d, 1H), 6.99 (dd, 1H), 7.98 (q, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569298B2
Source datasetuspto-grants-2013_10
ORD IDord-f2fc583b38fd4452815e9192b938d5d7
Source noteuspto-grants-2013_10