Dimethylformamide dimethyl acetal → 4-(1,1-Dimethylethyl)-2-dimethylaminomethyleneaminosulfonylanisole

HRID 364892Notes

Reaction equation

HRID 364892 reaction equation
[CH3:1][C:2]([C:5]1[CH:6]=[C:7]([S:13]([NH2:16])(=[O:15])=[O:14])[C:8]([O:11][CH3:12])=[CH:9][CH:10]=1)([CH3:4])[CH3:3].CO[CH:19](OC)[N:20]([CH3:22])[CH3:21]>CN(C)C=O>[CH3:4][C:2]([C:5]1[CH:10]=[CH:9][C:8]([O:11][CH3:12])=[C:7]([S:13]([N:16]=[CH:19][N:20]([CH3:22])[CH3:21])(=[O:15])=[O:14])[CH:6]=1)([CH3:1])[CH3:3]

Participants

4

Reactant 2

HCID 78373Dimethylformamide dimethyl acetalHCID 109336945-(Tert-butyl)-2-methoxybenzenesulfonamide

Product 1

HCID 544983284-(1,1-Dimethylethyl)-2-dimethylaminomethyleneaminosulfonylanisole

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

4.68 g (0.02 mole) of 3-(1,1-dimethylethyl)-6-methoxybenzenesulfonamide are dissolved in 50 ml of dimethylformamide, and 2.5 g (0.022 mole) of dimethylformamide dimethylacetal are added. The mixture is left to stand for 30 minutes at room temperature and is poured into ice water and the product is filtered off with suction.

Workup

  1. waitThe mixture is left
  2. filtrationthe product is filtered off with suction

Sources & evidence

ORD record
ord-c16d2080a66843218669fe2072e8e030
Source dataset
uspto-grants-1986_08
Patent number
US04607030

Reaction notes

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