Chloroacetone → 2,3-dihydro-2,2-dimethyl-6-(2-oxopropoxy)-4H-1,3-benzoxazin-4-one

HRID 1462352Notes

Reaction equation

HRID 1462352 reaction equation
[CH3:1][C:2]1([CH3:14])[NH:7][C:6](=[O:8])[C:5]2[CH:9]=[C:10]([OH:13])[CH:11]=[CH:12][C:4]=2[O:3]1.C(=O)([O-])[O-].[K+].[K+].Cl[CH2:22][C:23](=[O:25])[CH3:24]>C(#N)C>[CH3:1][C:2]1([CH3:14])[NH:7][C:6](=[O:8])[C:5]2[CH:9]=[C:10]([O:13][CH2:22][C:23](=[O:25])[CH3:24])[CH:11]=[CH:12][C:4]=2[O:3]1

Participants

5

Reactant 3

HCID 6571Chloroacetone2×HCID 11430Potassium CarbonateHCID 137543316-hydroxy-2,2-dimethyl-3,4-dihydro-2H-1,3-benzoxazin-4-one

Product 1

HCID 137543322,3-dihydro-2,2-dimethyl-6-(2-oxopropoxy)-4H-1,3-benzoxazin-4-one

Reagents, catalysts & solvents 1

HCID 6342AcetonitrileSolvent

Procedure

70 g of 2,3-dihydro-2,2-dimethyl-6-hydroxy-4H-1,3-benzoxazin-4-one in 400 ml of acetonitrile are stirred with 100 g of potassium carbonate and 32 ml of chloroacetone for 30 hours under reflux. After adding a further 3.2 ml of chloroacetone, the reaction mixture is heated for a further 15-20 hours. The reaction mixture is filtered whilst it is still warm, the residue is washed thoroughly with acetone and the combined filtrate is evaporated. The crystalline residue is recrystallised from toluene and yields 2,3-dihydro-2,2-dimethyl-6-(2-oxo-propoxy)-4H-1,3-benzoxazin-4-one with a melting point of 125°-126°.

Workup

  1. temperatureunder reflux
  2. temperaturethe reaction mixture is heated for a further 15-20 hours
  3. filtrationThe reaction mixture is filtered whilst it
  4. temperatureis still warm
  5. washthe residue is washed thoroughly with acetone
  6. customthe combined filtrate is evaporated
  7. customThe crystalline residue is recrystallised from toluene

Sources & evidence

ORD record
ord-e92a352f9cd04c2daeebb7f4a427dc61
Source dataset
uspto-grants-1984_07
Patent number
US04460580

Reaction notes

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