Dimethyl Sulfate → HCID 12807407, compound

HRID 1659597Notes

Reaction equation

HRID 1659597 reaction equation
[N+:1]([C:4]1[CH:9]=[C:8]([N+:10]([O-:12])=[O:11])[CH:7]=[C:6]([C:13]([F:16])([F:15])[F:14])[C:5]=1[NH:17][C:18]1[CH:23]=[CH:22][C:21]([O:24][C:25]([F:30])([F:29])[CH:26]([F:28])[F:27])=[CH:20][CH:19]=1)([O-:3])=[O:2].S(OC)(O[CH3:35])(=O)=O.C(=O)([O-])[O-].[Na+].[Na+]>CC(C)=O>[N+:1]([C:4]1[CH:9]=[C:8]([N+:10]([O-:12])=[O:11])[CH:7]=[C:6]([C:13]([F:16])([F:15])[F:14])[C:5]=1[N:17]([CH3:35])[C:18]1[CH:23]=[CH:22][C:21]([O:24][C:25]([F:29])([F:30])[CH:26]([F:28])[F:27])=[CH:20][CH:19]=1)([O-:3])=[O:2]

Participants

5

Procedure

Following the procedure of Example 18, N-(2,4-dinitro-6-trifluoromethylphenyl)-4-(1,1,2,2-tetrafluoroethoxy)benzenamine was reacted with dimethyl sulfate and sodium carbonate in acetone to provide N-(2,4-dinitro-6-trifluoromethylphenyl)-N-methyl-4-(1,1,2,2-tetrafluoroethoxy)benzenamine.

Sources & evidence

ORD record
ord-9cfa8ce45b7a474b9f860d4fd5f11400
Source dataset
uspto-grants-1981_12
Patent number
US04304791

Reaction notes

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