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4-Methyl-4-octylmorpholinium bromide → N-methyl-N-octylmorpholinium tetracyanoborate

HRID 1255108
Notes
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Reaction equation

HRID 1255108 reaction equation
[C:1]([B-:3]([C:8]#[N:9])([C:6]#[N:7])[C:4]#[N:5])#[N:2].[K+].[Br-].[CH3:12][N+:13]1([CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26])[CH2:18][CH2:17][O:16][CH2:15][CH2:14]1>>[C:1]([B-:3]([C:8]#[N:9])([C:6]#[N:7])[C:4]#[N:5])#[N:2].[CH3:12][N+:13]1([CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26])[CH2:18][CH2:17][O:16][CH2:15][CH2:14]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 204355134-Methyl-4-octylmorpholinium bromideHCID 23686396Potassium Tetracyanoborate

Product 1

HCID 86652226N-methyl-N-octylmorpholinium tetracyanoborate

Procedure

Analogously to Example A, 58 g of potassium tetracyanoborate are added to 100 g of 4-methyl-4-octylmorpholinium bromide, and the mixture is subjected to corresponding work-up, giving a clear, yellowish, viscous liquid.

Workup

  1. customgiving a clear, yellowish, viscous liquid

Sources & evidence

ORD record
ord-e428e9a9892e4301a6157fcb4c323c03
Source dataset
uspto-grants-2013_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08455703B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes