Lauryldimethylamine → N-(3-Chloropropyl)-N,N-dimethyl-1-dodecanaminium bromide

HRID 1245240

Reaction equation

[Br-:1].ClC[CH2:4][CH2:5][CH2:6][N+:7]([CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH3:21])([CH3:9])[CH3:8].[Br-].[Cl:23]CCCCCC[N+](CCCCCCCCCCCC)(C)C.C(N(C)C)CCCCCCCCCCC>>[Br-:1].[Cl:23][CH2:4][CH2:5][CH2:6][N+:7]([CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH3:21])([CH3:9])[CH3:8]

Participants

Reactant 3

HCID 8168Lauryldimethylamine

HCID 158701334-Chlorobutyldimethyldodecylammonium bromide

HCID 85711146(6-Chlorohexyl)dodecyldimethylammonium bromide

Product 1

HCID 10861601N-(3-Chloropropyl)-N,N-dimethyl-1-dodecanaminium bromide

Procedure

(4-Chlorobutyl)dodecyldimethylammonium bromide and (6-chlorohexyl) dodecyldimethylammonium bromide can be prepared by a similar process using the appropriate bromochloroalkane and dodecyldimethylamine.

Sources & evidence

ORD record: ord-478bb7d8c18d4f0f948fcdf080cbe919
Source dataset: uspto-grants-2006_10
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07125547B2

Linked notes

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