Potassium Hydroxide → HCID 53758222, compound
Reaction equation
[CH3:1][O:2][N:3]=[C:4]([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[CH2:13][O:14][C:15]1[CH:20]=[CH:19][CH:18]=[C:17]([Cl:21])[CH:16]=1)[C:5]#[N:6].[OH-:22].[K+]>>[CH3:1][O:2][N:3]=[C:4]([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[CH2:13][O:14][C:15]1[CH:20]=[CH:19][CH:18]=[C:17]([Cl:21])[CH:16]=1)[C:5]([NH2:6])=[O:22]Participants
3
Conditions
- Temperature
- 80 °C
Procedure
7.0 g (23 mmol) of 2-methoxyimino-2-[2-(m-chlorophenoxymethyl)-phenyl]acetonitrile were added to a mixture of 50 ml of glycol and 10 ml of a 25% by weight aqueous solution of potassium hydroxide, and the reaction mixture was then heated at 80° C. for 2 hours. The solid was then separated off, washed with methyl tert-butyl ether and dried. Yield: 58%;
Workup
- customThe solid was then separated off
- washwashed with methyl tert-butyl ether
- customdried
Sources & evidence
- ORD record
- ord-4f80c7e9a59044a4a064187ec3ad5608
- Source dataset
- uspto-grants-1997_10
- Patent number
- US05677347
Reaction notes
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