Methyl iodide → HCID 21436805, compound

HRID 2397875Notes

Reaction equation

[C:1]([O:18][CH2:19][C:20]([N:23]([CH3:25])[CH3:24])([CH3:22])[CH3:21])(=[O:17])[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].[CH3:26][I:27]>>[I-:27].[C:1]([O:18][CH2:19][C:20]([N+:23]([CH3:26])([CH3:25])[CH3:24])([CH3:21])[CH3:22])(=[O:17])[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]

Participants

Reactant 2

HCID 6328Methyl iodide

HCID 54128472HCID 54128472, compound

Product 1

HCID 21436805HCID 21436805, compound

Procedure

A 36 g portion of the ester obtained above was reacted with methyl iodide 15 g as described in Example 2. There was obtained (2-palmitoyloxy-1,1-dimethylethyl)-trimethylammonium iodide, m.p. 170.8° C.

Sources & evidence

ORD record: ord-06049fbb642640488dd7c21da5f8d6b2
Source dataset: uspto-grants-1977_05
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04022909

Reaction notes

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