4-Nitrobenzyl bromide → HCID 178443149, compound

HRID 1706390Notes

Reaction equation

HRID 1706390 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][CH3:21])[N:3]=1.[N+:22]([C:25]1[CH:32]=[CH:31][C:28]([CH2:29][Br:30])=[CH:27][CH:26]=1)([O-:24])=[O:23]>>[Br-:30].[CH3:1][C:2]1[N:3]([CH2:29][C:28]2[CH:31]=[CH:32][C:25]([N+:22]([O-:24])=[O:23])=[CH:26][CH:27]=2)[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][CH3:21])=[C:5]([CH3:7])[CH:6]=1

Participants

3

Reactant 2

HCID 660114-Nitrobenzyl bromideHCID 20335964HCID 20335964, compound

Product 1

HCID 178443149HCID 178443149, compound

Procedure

Reaction of 3,5-dimethyl-1-tetradecyl-pyrazole with 4-nitrobenzyl bromide yields 3,5-dimethyl-2(4-nitrobenzyl)-1-tetradecyl-pyrazolium bromide; m.p. 159°-161° C.

Sources & evidence

ORD record
ord-abe491177f94407b8cdc9226e934a9b2
Source dataset
uspto-grants-1980_06
Patent number
US04207326

Reaction notes

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