Water → 4-Chloro-2-[[(1-methylethylidene)amino]oxy]benzonitrile

HRID 2396719Notes

Reaction equation

HRID 2396719 reaction equation
[CH3:1][C:2](=[N:4][OH:5])[CH3:3].[K].[Cl:7][C:8]1[CH:15]=[CH:14][C:11]([C:12]#[N:13])=[C:10]([N+]([O-])=O)[CH:9]=1.O>CN(C)C=O>[Cl:7][C:8]1[CH:15]=[CH:14][C:11]([C:12]#[N:13])=[C:10]([O:5][N:4]=[C:2]([CH3:3])[CH3:1])[CH:9]=1

Participants

6

Reactant 4

HCID 962WaterHCID 67180Acetone, oximeHCID 969244-Chloro-2-nitrobenzonitrileHCID 5462222Potassium

Product 1

HCID 187964524-Chloro-2-[[(1-methylethylidene)amino]oxy]benzonitrileYield 65.6%

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

In 75 ml of dry N,N-dimethylformamide was dissolved acetone oxime (1.21 g), followed by potassium tertiaryl butoxide (1.85 g) and stirred under nitrogen. After 30 minutes, 4-chloro-2-nitro-benzonitrile (2.00 g) was added. After an additional 30 minutes the reaction was poured into water (500 ml) and filtered. The solid was collected and dissolved in DCM (250 ml), dried (MgSO4), and concentrated in vacuo. The resulting solid was recrystallized from ethanol to yield 1.5 g of the product, m.p. 83°-84° C.

Workup

  1. filtrationfiltered
  2. customThe solid was collected
  3. dissolutiondissolved in DCM (250 ml)
  4. dry with materialdried (MgSO4)
  5. concentrationconcentrated in vacuo
  6. customThe resulting solid was recrystallized from ethanol

Sources & evidence

ORD record
ord-c2bb2f5f3a8a43a7961d29a3302ac8f0
Source dataset
uspto-grants-1996_02
Patent number
US05494908

Reaction notes

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