Itaconic acid → HCID 68747579, compound

HRID 1801406Notes

Reaction equation

[CH2:1]([NH2:19])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8]/[CH:9]=[CH:10]\[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18].[C:20]([OH:28])(=[O:27])[C:21]([CH2:23][C:24](O)=[O:25])=[CH2:22].[NH2:29][CH2:30][CH2:31][O:32][CH2:33][CH2:34][OH:35]>>[OH:35][CH2:34][CH2:33][O:32][CH2:31][CH2:30][NH3+:29].[CH2:1]([N:19]1[C:24](=[O:25])[CH2:23][CH:21]([C:20]([O-:28])=[O:27])[CH2:22]1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8]/[CH:9]=[CH:10]\[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18]

Participants

Reactant 3

HCID 811Itaconic acid

HCID 13578Diglycolamine

HCID 5356789Oleylamine

Product 1

HCID 68747579HCID 68747579, compoundYield 101%

Procedure

265 g of oleylamine, 130 g of itaconic acid and 105 g of 2-(2-aminoethoxy)ethanol were used to obtain 485 g of N-oleyl-5-oxopyrrolidine-3-carboxylic acid 2-(2-hydroxyethoxy)ethylammonium salt with

Sources & evidence

ORD record: ord-07cce07920c8470cbd5dc1e2103c99ea
Source dataset: uspto-grants-2013_01
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08349215B2

Reaction notes

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