Potassium → 2-(Hydroxyimino)-2-phenylacetonitrile
Reaction equation
[K].[OH:2][N:3]=[C:4]([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1COC1C=C(C)C=CC=1C)[C:5]#[N:6].CC1C=CC(C)=CC=1OCC1C=CC=CC=1COC1C=C(C)C=CC=1C>C1(C)C=CC=CC=1>[OH:2][N:3]=[C:4]([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)[C:5]#[N:6]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Thus, 1262.7 g of an aqueous solution containing 189.1 g (0.594 mol, 95.8% yield, E/Z=15/85) of the potassium salt of α-hydroxyimino-2-(2,5-dimethylphenoxymethyl)phenylacetonitrile was obtained. It was found that 1,2-bis(2,5-dimethylphenoxymethyl)benzene was not found in the aqueous solution, but contained at an amount of 33.7 g (0.097 mol, 96.1% recovery) in 594 g of toluene after washing.
Workup
- customwas obtained
- washafter washing
Sources & evidence
- ORD record
- ord-ed5013acf4444532a0116e640392bd5e
- Source dataset
- uspto-grants-1996_04
- Patent number
- US05510506
Reaction notes
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