Dimethyl Sulfate → HCID 20572385, compound
Reaction equation
[F:1][C:2]([F:13])([F:12])[CH2:3][NH:4][C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([CH3:11])[CH:6]=1.[C:14](=O)(O)[O-].[Na+].S(OC)(OC)(=O)=O>>[CH3:14][N:4]([CH2:3][C:2]([F:12])([F:13])[F:1])[C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([CH3:11])[CH:6]=1Participants
4
Procedure
The same method as in Example 2 is carried out using 56.7 parts of N-(2,2,2-trifluoroethyl)-m-toluidine, 53 parts of sodium bicarbonate and 75 parts of dimethyl sulphate. 52.8 parts, i.e. a yield equal to 86.7% of the theoretical yield, of N-methyl N-(2,2,2-trifluoroethyl)-m-toluidine are obtained.
Sources & evidence
- ORD record
- ord-663f9ac7afe34269afccae55159f719e
- Source dataset
- uspto-grants-1981_08
- Patent number
- US04285696
Reaction notes
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