Methyl Bromide → N-isononyl-N,N-dimethyl decanaminium chloride

HRID 486115Notes

Reaction equation

C(N(CCCCCCCCC)C)CCCCCCCCC.[Cl-:22].C([N+](CCCCCCCCC)(C)C)CCCCCCCCC.CBr.CI.CCl.[Br-].[CH2:52]([N+:62]([CH2:65][CH2:66][CH2:67][CH2:68][CH2:69][CH2:70][CH:71]([CH3:73])[CH3:72])([CH3:64])[CH3:63])[CH2:53][CH2:54][CH2:55][CH2:56][CH2:57][CH2:58][CH2:59][CH2:60][CH3:61].[I-].C([N+](CCCCCCC(C)C)(C)C)CCCCCCCCC>>[Cl-:22].[CH2:52]([N+:62]([CH2:65][CH2:66][CH2:67][CH2:68][CH2:69][CH2:70][CH:71]([CH3:72])[CH3:73])([CH3:64])[CH3:63])[CH2:53][CH2:54][CH2:55][CH2:56][CH2:57][CH2:58][CH2:59][CH2:60][CH3:61]

Participants

Reactant 7

HCID 6323Methyl Bromide

HCID 6327Methyl Chloride

HCID 6328Methyl iodide

HCID 19937971HCID 19937971, compound

HCID 19937975HCID 19937975, compound

HCID 23185420HCID 23185420, compound

HCID 53874927HCID 53874927, compound

Product 1

HCID 9950184N-isononyl-N,N-dimethyl decanaminium chloride

Procedure

When decylnonylmethylamine is used instead of decylisononylmethylamine, the product is decylnonyldimethylammonium chloride. Similarly, when methyl bromide or methyl iodide are used instead of methyl chloride, the products are decylisononyldimethylammonium bromide and decylisononyldimethylammonium iodide, respectively.

Sources & evidence

ORD record: ord-aa85433795194f16b874728c19769cb3
Source dataset: uspto-grants-1994_03
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05290805

Reaction notes

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