Methyl iodide → HCID 15008680, compound

HRID 1761395Notes

Reaction equation

HRID 1761395 reaction equation
[Br:1][C:2]1[CH:20]=[C:19]([N+:21]([O-:23])=[O:22])[CH:18]=[CH:17][C:3]=1[NH:4][C:5](=[O:16])[C:6]([F:15])([C:11]([F:14])([F:13])[F:12])[C:7]([F:10])([F:9])[F:8].CI.[C:26](=O)([O-])[O-].[K+].[K+]>CC(C)=O>[CH3:26][N:4]([C:5](=[O:16])[C:6]([F:15])([C:11]([F:12])([F:13])[F:14])[C:7]([F:8])([F:9])[F:10])[C:3]1[CH:17]=[CH:18][C:19]([N+:21]([O-:23])=[O:22])=[CH:20][C:2]=1[Br:1]

Participants

5

Reactant 3

HCID 6328Methyl iodideHCID 11430Potassium CarbonateHCID 163755N-(2-Bromo-4-nitrophenyl)-2,3,3,3-tetrafluoro-2-(trifluoromethyl)propanamide

Product 1

HCID 15008680HCID 15008680, compoundYield 70%

Reagents, catalysts & solvents 1

HCID 180AcetoneSolvent

Procedure

2'-Bromo-4'-nitro-2,3,3,3-tetrafluoro-2-(trifluoromethyl)propionanilide was reacted with methyl iodide, in acetone and in the presence of potassium carbonate, yielding N-methyl-2'-bromo-4'-nitro-2,3,3,3-tetrafluoro-2-(trifluoromethyl)propionanilide, an oil, yield 70% (>99% branched isomer).

Sources & evidence

ORD record
ord-718cfc3e9bc249378ecf93e16ac54705
Source dataset
uspto-grants-1989_05
Patent number
US04826841

Reaction notes

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