Anthranilic Acid → Propylamine
Reaction equation
[C:1]([OH:8])(=[O:7])/[CH:2]=[CH:3]\[C:4]([OH:6])=O.C1(=O)O[C:12](=O)[CH:11]=C1.[NH2:16]CC(O)=O.N[C@H](C(O)=O)CCC(O)=O.N[C@H](C(O)=O)C.N1CCC[C@H]1C(O)=O.C(O)(=O)C1C(=CC=CC=1)N.S(O)(=O)(C1C=CC(N)=CC=1)=O.NC1C=CC=C(C)C=1S(O)(=O)=O.C1C=CC2C=C(N)C=CC=2C=1>>[C:4]1(=[O:6])[O:8][C:1](=[O:7])[CH:2]=[CH:3]1.[CH2:3]([NH2:16])[CH2:2][CH3:1].[CH2:1]([NH2:16])[CH2:2][CH2:3][CH3:4].[NH:16]1[CH2:3][CH2:4][O:6][CH2:12][CH2:11]1Participants
14
Reactant 10
Product 4
Procedure
Examples of monomers which can provide structure units represented by Formula (4) include half amides of maleic acid, prepared by the reaction of maleic anhydride with glycine, glutamic acid, alanine, proline, anthranilic acid or by the reaction of maleic anhydride with sulfanilic acid, amino-toluene sulfonic acid, naphthylamine-monosulfonic acid or naphthylamine disulfonic acid and the halfamides obtained by the reaction of maleic anhydride with N-propylamine, N-butylamine, morpholine or amino alkanoles.
Sources & evidence
- ORD record
- ord-7124bdd5272a4ae488ccd70f9adb1d70
- Source dataset
- uspto-grants-1997_05
- Patent number
- US05633310
Reaction notes
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