N-Hydroxyphthalimide → 0-(5-Nitro-6-quinolyl)-phthalimide

Reaktionsgleichung

O[N:2]1[C:6](=[O:7])[C:5]2=[CH:8][CH:9]=[CH:10][CH:11]=[C:4]2[C:3]1=[O:12].[N+:13]([C:16]1[C:25](Cl)=[CH:24][CH:23]=[C:22]2[C:17]=1[CH:18]=[CH:19][CH:20]=[N:21]2)([O-:15])=[O:14]>>[N+:13]([C:16]1[C:25]([C:5]23[CH:8]=[CH:9][CH:10]=[CH:11][CH:4]2[C:3]([NH:2][C:6]3=[O:7])=[O:12])=[CH:24][CH:23]=[C:22]2[C:17]=1[CH:18]=[CH:19][CH:20]=[N:21]2)([O-:15])=[O:14]

Komponenten

Edukt 2

HCID 10665N-Hydroxyphthalimide

HCID 40708006-Chloro-5-nitroquinoline

Produkt 1

HCID 1317158270-(5-Nitro-6-quinolyl)-phthalimide

Versuchsvorschrift

N-hydroxy-phthalimide and 5-nitro-6-chloro-quinoline were reacted to form 0-(5-nitro-6-quinolyl)-phthalimide melting at 185° C. which was reacted to obtain 0-(5-nitro-6-quinolyl)hydroxylamine melting at 165° C.

Quellen und Nachweise

ORD-Eintrag: ord-e384b9c723e44557b65d3f2f0d4d7dd2
Quelldatensatz: uspto-grants-1989_01
DOI: 10.6084/m9.figshare.5104873.v1
Patentnummer: US04801717

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