Nitric Acid → HCID 19034857、化合物

HRID 1641473ノート

反応式

HRID 1641473 の反応式
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

参加物

8

実験手順

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.

出典と根拠

ORDレコード
ord-fd392b602278403ab168bc483df5eb2c
出典データセット
uspto-grants-2012_02
特許番号
US08115007B2

反応ノート

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