Ethyl Bromide → HCID 20335959, compound

HRID 1706384Notes

Reaction equation

[CH2:1]([N:17]1[C:21]([CH3:22])=[CH:20][C:19]([CH3:23])=[N:18]1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16].[CH2:24]([Br:26])[CH3:25]>>[Br-:26].[CH2:24]([N:18]1[C:19]([CH3:23])=[CH:20][C:21]([CH3:22])=[N+:17]1[CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16])[CH3:25]

Participants

Reactant 2

HCID 6332Ethyl Bromide

HCID 5728953,5-Dimethyl-1-hexadecylpyrazole

Product 1

HCID 20335959HCID 20335959, compound

Procedure

In the same way as described in Example 4-A, reaction of 1-hexadecyl-3,5-dimethyl-pyrazole with ethyl bromide yields 2-ethyl-1-hexadecyl-3,5-dimethyl-pyrazolium bromide; m.p. 97°-101° C.

Sources & evidence

ORD record: ord-28cb820df0de43ad946b9d0a5ab777f0
Source dataset: uspto-grants-1980_06
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04207326

Reaction notes

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