Maleic Anhydride → HCID 86743662, compound
Reaction equation
CO[C:3](=[O:5])[O-:4].[CH3:6][N+:7]([CH2:12][CH3:13])([CH2:10][CH3:11])[CH2:8][CH3:9].C1(=O)[O:19][C:17](=[O:18])[CH:16]=[CH:15]1>O>[C:3]([O-:4])(=[O:5])/[CH:15]=[CH:16]\[C:17]([O-:19])=[O:18].[CH3:6][N+:7]([CH2:12][CH3:13])([CH2:10][CH3:11])[CH2:8][CH3:9].[CH3:6][N+:7]([CH2:12][CH3:13])([CH2:10][CH3:11])[CH2:8][CH3:9]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
By following the same procedure as Example 20 (2nd step) except that 8.8 g of methyltriethylammonium methyl carbonate, 8.8 g of water, and 4.5 g of maleic anhydride were used, 10.6 g (yield of 100%) of methyltriethylammonium maleate was obtained. The content of monomethyl maleate was less than 0.15 and the contents of impurity ions were all less than 1 ppm.
Sources & evidence
- ORD record
- ord-957c35faaf5249d5a490456cf7a174ae
- Source dataset
- uspto-grants-1990_01
- Patent number
- US04892944
Reaction notes
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