Nitric Acid → HCID 19034857, Verbindung

HRID 1641473Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1641473
N[C:2]1[C:3]([NH2:14])=[C:4]([N+:11]([O-:13])=[O:12])[C:5]([N+]([O-])=O)=[N:6][CH:7]=1.N[C:16]1[CH:21]=[CH:20][C:19]([N+]([O-])=O)=[C:18]([N+:25]([O-:27])=[O:26])[C:17]=1[NH2:28].NC1C=CC=CN=1.NC1C=CC=CC=1.[OH:43][S:44](O)(=[O:46])=[O:45].[O:48]=[S:49](=[O:51])=[O:50].[N+]([O-])(O)=O>>[NH2:14][C:3]1[CH:2]=[CH:7][N:6]=[C:5]([S:44]([OH:46])(=[O:45])=[O:43])[C:4]=1[N+:11]([O-:13])=[O:12].[NH2:28][C:17]1[C:18]([N+:25]([O-:27])=[O:26])=[C:19]([S:49]([OH:51])(=[O:50])=[O:48])[CH:20]=[CH:21][CH:16]=1

Komponenten

8

Versuchsvorschrift

The present invention comprises a process for the preparation of 1) diaminodinitropyridine or 2) diaminodinitrobenzene by contacting 1) an aminopyridine or 2) an aminobenzene, respectively, with oleum and nitric acid, wherein the improvement comprises adding at least about 1% molar excess of nitric acid based upon the aminopyridine or aminobenzene respectively, with stirring for at least two hours to form first 1) aminonitropyridine sulfonic acid or 2) aminonitrobenzene sulfonic acid, respectively, and then 1) diaminodinitropyridine or 2) diaminodinitrobenzene respectively.

Quellen und Nachweise

ORD-Eintrag
ord-fd392b602278403ab168bc483df5eb2c
Quelldatensatz
uspto-grants-2012_02
Patentnummer
US08115007B2

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