Sodium Hydroxide → phenyl N-[3-(dimethylcarbamoyl)phenyl]carbamate
Reaction equation
[NH2:1][C:2]1[CH:3]=[C:4]([CH:10]=[CH:11][CH:12]=1)[C:5]([N:7]([CH3:9])[CH3:8])=[O:6].[OH-].[Na+].Cl[C:16]([O:18][C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1)=[O:17]>O1CCOCC1>[CH3:8][N:7]([CH3:9])[C:5]([C:4]1[CH:3]=[C:2]([NH:1][C:16](=[O:17])[O:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[CH:12]=[CH:11][CH:10]=1)=[O:6]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a stirred solution of 3-amino-N,N-dimethylbenzamide (1.3 g) in 1,4-dioxane(20 ml) was added 1N sodium hydroxide (23.4 ml) and phenyl chloroformate (1.5 ml) successively in an ice-cooled bath. The bath was removed and the reaction mixture was stirred vigorously for 3 hours during which time, phenyl chloroformate (0.7 ml) was further added. The mixture was extracted with ethyl acetate and the organic layer was washed with water and saturated sodium chloride solution. After dried over anhydrous magnesium sulfate and filtered, the solvent was removed in vacuo and the residual oil was purified by flash chromatography eluting with ethyl acetate-n-hexane (2:1, V/V) to give a solid, which was recrystallized from benzene-n-hexane (5:1, V/V) to afford phenyl 3-(dimethylcarbamoyl)phenylcarbamate (1.4 g) as a colorless powder.
Workup
- temperaturecooled bath
- customThe bath was removed
- additionwas further added
- extractionThe mixture was extracted with ethyl acetate
- washthe organic layer was washed with water and saturated sodium chloride solution
- dry with materialAfter dried over anhydrous magnesium sulfate
- filtrationfiltered
- customthe solvent was removed in vacuo
- customthe residual oil was purified by flash chromatography
- washeluting with ethyl acetate-n-hexane (2:1, V/V)
- customto give a solid, which
- customwas recrystallized from benzene-n-hexane (5:1, V/V)
Sources & evidence
- ORD record
- ord-8473e907ab6c4ce0bc76ec05760c7a36
- Source dataset
- uspto-grants-1996_10
- Patent number
- US05563162
Reaction notes
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