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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 483224Generated: October 26, 2026

Ethyl benzoylacetate → 2-amino-6-phenyl-4H-1,3-oxazin-4-one

https://huagongshe.com/reaction/483224

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl benzoylacetateHCID 7170—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 178485225HCID 178485225—
SolventWaterHCID 962—
Product2-amino-6-phenyl-4H-1,3-oxazin-4-oneHCID 1337093476.2%

Reaction Steps

To 9.45 g (0.034M) of methylthiopseudourea H2SO4 is added 40.0 ml of H2O+8.0 g (0.142M) of KOH. With vigorous stirring, 12.0 g (0.0625M) of ethyl benzoylacetate (Aldrich) is also added and the heterogenous mixture allowed to stir at ambient temperature for 18 hours. The resulting solids are filtered and washed very well with H2O followed by ether. The solids are dried at 60° C. in a vacuum oven to yield 7.20 g (61.3 percent) of 2-amino-6-phenyl-1,3-oxazine-4-one. An analytical sample is recrystallized from 95 percent EtOH:DMF to yield 2-amino-6-phenyl-1,3-oxazine-4-one (m.p. 244-246 d).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04578466
Source datasetuspto-grants-1986_03
ORD IDord-00c3066bcb3c40ef889b3a4e43f42999
Source noteuspto-grants-1986_03