Methyl p-toluenesulfonate → HCID 178443023, compound
Reaction equation
[CH3:1][C:2]1[CH:6]=[C:5]([CH3:7])[N:4]([CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23])[N:3]=1.[CH3:24][O:25][S:26]([C:29]1[CH:34]=[CH:33][C:32]([CH3:35])=[CH:31][CH:30]=1)(=[O:28])=[O:27]>>[C:32]1([CH3:35])[CH:31]=[CH:30][C:29]([S:26]([O-:28])(=[O:25])=[O:27])=[CH:34][CH:33]=1.[CH2:8]([N+:4]1[N:3]([CH3:24])[C:2]([CH3:1])=[CH:6][C:5]=1[CH3:7])[CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23]Participants
3
Procedure
Reaction of 3,5-dimethyl-1-hexadecyl-pyrazole with toluene-4-sulfonic acid-methyl ester yields 1-hexadecyl-2,3,5-trimethylpyrazolium p-toluene sulfonate; m.p. 113°-114° C.
Sources & evidence
- ORD record
- ord-49a37934a5ba44abb4125902ad055e8c
- Source dataset
- uspto-grants-1980_06
- Patent number
- US04207326
Reaction notes
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