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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234888Generated: October 25, 2026

Ethyl Acetate → Methyl 3,4-dihydro-2,2-dimethyl-3-oxo-2H-1,4-benzoxazine-7-carboxylate

https://huagongshe.com/reaction/234888

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant2-Bromo-2-methylpropionyl bromideHCID 88685—
ReactantSodium BicarbonateHCID 516892—
ReactantBenzoic acid, 4-amino-3-hydroxy-, methyl esterHCID 7020619—
SolventWaterHCID 962—
ProductMethyl 3,4-dihydro-2,2-dimethyl-3-oxo-2H-1,4-benzoxazine-7-carboxylateHCID 1058582078.3%

Reaction Steps

To a solution of 2-amino-5-methoxycarbonylphenol [Tetrahedron, 46(15), 5177-5186 (1990)] (9.8 g) in a mixed solvent of ethyl acetate (200 ml) and water (200 ml) were added sodium hydrogen carbonate (7.3 g) and 2-bromoisobutyryl bromide (13.7 g) and the mixture was stirred at room temperature for 10 minutes. The organic layer was separated and the solvent was distilled off under reduced pressure. The resulting residue was dissolved in dimethylformamide (500 ml), to the solution was added potassium carbonate (8.9 g) and the mixture was stirred at room temperature for a day. The reaction solution was poured into water to give precipitates, which were taken by filtration and dried to give 2,2-dimethyl-7-methoxycarbonyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazine (10.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05597820
Source datasetuspto-grants-1997_01
ORD IDord-78780060dd4243b1a4b2f825c06e229a
Source noteuspto-grants-1997_01