9,10-Anthracenedione, 1,5-dinitro- → 9,10-Anthracenedione, 1,5-dinitro-

HRID 128159

Reaction equation

HRID 128159 reaction equation
[N+:1]([C:4]1[C:17]2[C:16](=[O:18])[C:15]3[C:10](=[C:11]([N+:19]([O-:21])=[O:20])[CH:12]=[CH:13][CH:14]=3)[C:9](=[O:22])[C:8]=2[CH:7]=[CH:6][CH:5]=1)([O-:3])=[O:2].[N+:23]([C:26]1[C:39]2[C:38](=[O:40])[C:37]3[C:32](=[CH:33][CH:34]=[CH:35][C:36]=3[N+:41]([O-:43])=[O:42])[C:31](=[O:44])[C:30]=2[CH:29]=[CH:28][CH:27]=1)([O-:25])=[O:24]>>[N+:1]([C:4]1[C:17]2[C:16](=[O:18])[C:15]3[C:10](=[C:11]([N+:19]([O-:21])=[O:20])[CH:12]=[CH:13][CH:14]=3)[C:9](=[O:22])[C:8]=2[CH:7]=[CH:6][CH:5]=1)([O-:3])=[O:2].[N+:23]([C:26]1[C:39]2[C:38](=[O:40])[C:37]3[C:32](=[CH:33][CH:34]=[CH:35][C:36]=3[N+:41]([O-:43])=[O:42])[C:31](=[O:44])[C:30]=2[CH:29]=[CH:28][CH:27]=1)([O-:25])=[O:24].[N+:1]([C:4]1[C:17]2[C:16](=[O:18])[C:15]3[C:10](=[C:11]([N+:19]([O-:21])=[O:20])[CH:12]=[CH:13][CH:14]=3)[C:9](=[O:22])[C:8]=2[CH:7]=[CH:6][CH:5]=1)([O-:3])=[O:2].[N+:23]([C:14]1[C:15]2[C:16](=[O:18])[C:17]3[C:8](=[CH:7][CH:6]=[CH:5][C:4]=3[N+:1]([O-:3])=[O:2])[C:9](=[O:22])[C:10]=2[CH:11]=[CH:12][CH:13]=1)([O-:25])=[O:24]

Participants

5

Reactant 2

HCID 67059,10-Anthracenedione, 1,5-dinitro-HCID 672101,8-Dinitro-9,10-anthraquinone

Product 3

HCID 67059,10-Anthracenedione, 1,5-dinitro-HCID 672101,8-Dinitro-9,10-anthraquinoneHCID 205683081,8-Dinitroanthraquinone 1,5-dinitroanthraquinone

Procedure

Calculation: theoretical yield from Σanthraquinone and 1-nitroanthraquinone related to 1,5-dinitroanthraquinone and 1,8-dinitroanthraquinone formed (-total 1,5-dinitroanthraquinone and 1,8-dinitroanthraquinone -1,5-dinitroanthraquinone and 1,8-dinitroanthraquinone employed).

Sources & evidence

ORD record
ord-a6524727cc1b49aa9c768f4ed817636c
Source dataset
uspto-grants-1981_03
Patent number
US04259248

Linked notes

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