Reaction equation
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][C:2]1=[O:10].[C:11](Cl)(=[O:13])[CH3:12].O>ClCCCl>[C:11]([C:6]1[CH:5]=[C:4]2[C:9](=[CH:8][CH:7]=1)[NH:1][C:2](=[O:10])[CH2:3]2)(=[O:13])[CH3:12]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 50 °C
Procedure
2-Oxindole (3 g) was suspended in 1,2-dichloroethane and slowly treated with 3.2 ml of acetyl chloride. The resulting suspension was heated at 50° C. for 5 hours, cooled, and poured into water. The resulting precipitate was collected by vacuum filtration, washed copiously with water and dried under vacuum to give 2.9 g (73% yield) of 5-acetyl-2-oxindole as a brown solid.
Workup
- temperaturecooled
- filtrationThe resulting precipitate was collected by vacuum filtration
- washwashed copiously with water
- customdried under vacuum
Sources & evidence
- ORD record
- ord-99041ee34924491abeb4187799fa7c5f
- Source dataset
- uspto-grants-2005_02
- Patent number
- US06855730B2
Linked notes
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