1-(Bromomethyl)-4-chlorobenzene → HCID 178443221, 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][CH3:19])[N:3]=1.[Cl:20][C:21]1[CH:28]=[CH:27][C:24]([CH2:25][Br:26])=[CH:23][CH:22]=1>>[Br-:26].[Cl:20][C:21]1[CH:28]=[CH:27][C:24]([CH2:25][N:3]2[C:2]([CH3:1])=[CH:6][C:5]([CH3:7])=[N+:4]2[CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH3:19])=[CH:23][CH:22]=1Participants
3
Procedure
Reaction of 3,5-dimethyl-1-dodecyl-pyrazole with p-chlorobenzyl bromide yields 2-(p-chlorobenzyl)-3,5-dimethyl-1-dodecyl-pyrazolium bromide; m.p. 166.5°-167.5° C.
Sources & evidence
- ORD record
- ord-c6efa3feb93d4d8bbed98fa46ae07b4e
- Source dataset
- uspto-grants-1980_06
- Patent number
- US04207326
Reaction notes
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