Succinimide → Aspartate Succinimide

HRID 736018Notes

Reaction equation

HRID 736018 reaction equation
[NH2:1][C@H:2]([C:7]([O-:9])=[O:8])[CH2:3][C:4]([O-:6])=[O:5].[C:10]1(=[O:16])[NH:14][C:13](=[O:15])[CH2:12][CH2:11]1>>[NH2:1][C@H:2]([C:7]([O-:9])=[O:8])[CH2:3][C:4]([O-:6])=[O:5].[C:13]1(=[O:15])[NH:14][C:10](=[O:16])[CH2:11][CH2:12]1

Participants

3

Reactant 2

HCID 11439Succinimide2×HCID 5460541l-aspartic acid, sodium salt

Product 1

HCID 86612006Aspartate Succinimide

Procedure

The procedure was repeated using 2.05 g of MgSO4 heptahydrate (8.33 mmol Mg2+ and SO42−, equivalent to 16.7 mmol each of cations and anions). Upon drying, this is expected to produce about 83.3 mmol of Asp as the ammonium aspartate, with 16.7 mmol as Mg aspartate. In this case, the target upon polymerization was a copolymer of aspartate and succinimide with a 1:5 residue ratio. The product had a residue ratio of about 20% Mg aspartate and 80% succinimide (1:4) and was largely insoluble. The molecular weight as shown by gel permeation was approximately 1500 Daltons.

Workup

  1. customIn this case, the target upon polymerization

Sources & evidence

ORD record
ord-a2cf3e33cb244bfaa1627576e517a58c
Source dataset
uspto-grants-2009_09
Patent number
US07595007B2

Reaction notes

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