Maleic Anhydride → HCID 86743663, compound
Reaction equation
CO[C:3](=[O:5])[O-:4].[CH2:6]([N+:8]([CH3:11])([CH3:10])[CH3:9])[CH3:7].C1(=O)[O:17][C:15](=[O:16])[CH:14]=[CH:13]1>O>[C:3]([O-:4])(=[O:5])/[CH:13]=[CH:14]\[C:15]([O-:17])=[O:16].[CH2:6]([N+:8]([CH3:11])([CH3:10])[CH3:9])[CH3:7].[CH2:6]([N+:8]([CH3:11])([CH3:10])[CH3:9])[CH3:7]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
By following the same procedure as Example 20 (2nd step) except that 7.8 g of ethyltrimethylammonium methyl carbonate, 7.8 g of water, and 4.7 g of maleic anhydride were used, 9.7 g (yield of 99.9%) of ethyltrimethylammonium maleate was obtained. The content of monomethyl maleate was less than 0.1% and the contents of impurity ions were all less than 1 ppm.
Sources & evidence
- ORD record
- ord-745397045b81496da13d517800d765b4
- Source dataset
- uspto-grants-1990_01
- Patent number
- US04892944
Reaction notes
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