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

HRID 2413028Notes

Reaction equation

HRID 2413028 reaction equation
C[NH:2][C:3](=[NH:5])S.OS(O)(=O)=O.[OH-].[K+].[C:13]([CH2:21][C:22]([O:24]CC)=O)(=[O:20])[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1>O>[NH2:5][C:3]1[O:20][C:13]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)=[CH:21][C:22](=[O:24])[N:2]=1

Participants

5

Reactant 3

HCID 7170Ethyl benzoylacetateHCID 14797Potassium HydroxideHCID 178485225HCID 178485225, compound

Product 1

HCID 133709342-amino-6-phenyl-4H-1,3-oxazin-4-oneYield 76.2%

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

To 9.45 g (0.034 M) of methylthiopseudourea H2SO4 is added 40.0 ml of H2O+8.0 g (0.142 M) of KOH. With vigorous stirring, 12.0 g (0.0625 M) 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).

Workup

  1. filtrationThe resulting solids are filtered
  2. washwashed very well with H2O
  3. customThe solids are dried at 60° C. in a vacuum oven

Sources & evidence

ORD record
ord-839c982fd00b4b24b8b7150b2a0c6295
Source dataset
uspto-grants-1985_01
Patent number
US04495349

Reaction notes

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