Benzyl Bromide → HCID 178442893, compound

HRID 1706387Notes

Reaction equation

HRID 1706387 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][CH2:23][CH2:24][CH3:25])[N:3]=1.[CH2:26]([Br:33])[C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1>>[Br-:33].[CH2:26]([N:3]1[C:2]([CH3:1])=[CH:6][C:5]([CH3:7])=[N+:4]1[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][CH2:23][CH2:24][CH3:25])[C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1

Participants

3

Procedure

Reaction of 3,5-dimethyl-1-octadecyl-pyrazole with benzyl bromide yields 2-benzyl-3,5-dimethyl-1-octadecyl-pyrazolium bromide; m.p. 165.5°-167.5° C.

Sources & evidence

ORD record
ord-2b3e3e73345e40658bb659650539c0b4
Source dataset
uspto-grants-1980_06
Patent number
US04207326

Reaction notes

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