Water → Ethanediamide, N1,N2-bis(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-

HRID 1447746

Reaktionsgleichung

Reaktionsgleichung von HRID 1447746
[C:1]1(=[O:11])O[C:4](=[O:5])[C:3]2=[CH:7][CH:8]=[CH:9][CH:10]=[C:2]12.[C:12]([NH:18][NH2:19])(=[O:17])[C:13]([NH:15][NH2:16])=[O:14].[OH2:20]>C1(C)C(C)=CC=CC=1>[C:4]1(=[O:5])[N:16]([NH:15][C:13]([C:12]([NH:18][N:19]2[C:1](=[O:11])[C:2]3=[CH:10][CH:9]=[CH:8][CH:7]=[C:3]3[C:4]2=[O:5])=[O:17])=[O:14])[C:1](=[O:20])[C:2]2=[CH:10][CH:9]=[CH:8][CH:7]=[C:3]12

Komponenten

5

Edukt 3

HCID 962WaterHCID 6811Phthalic AnhydrideHCID 13826Oxalic acid, dihydrazide

Produkt 1

HCID 113193Ethanediamide, N1,N2-bis(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-Ausbeute 94 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 7237O-XyleneLösungsmittel

Versuchsvorschrift

Two moles of phthalic anhydride (296 g) and one mole of oxalic dihydrazide (118 g) in xylene (2.5 l) were heated at reflux until two moles of water were removed (about 24 hours). The product was filtered and dried at 50° C. N,N'-bis(phthalimido)oxamide was obtained in 94-6 percent yield. The compound was a white solid melting at 295° C. (dec.) and having the following elemental analysis by weight percent:

Aufarbeitung

  1. customwere removed (about 24 hours)
  2. filtrationThe product was filtered
  3. customdried at 50° C

Quellen und Nachweise

ORD-Eintrag
ord-11ee881c856b499e88390e089f2b5f81
Quelldatensatz
uspto-grants-1979_12
Patentnummer
US04178280

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