1-Nitroanthraquinone → HCID 178514954, compound
Reaction equation
NN.[N+:3]([C:6]1[C:19]2[C:18](=[O:20])[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[C:11](=[O:21])[C:10]=2[CH:9]=[CH:8][CH:7]=1)([O-])=[O:4]>>[OH:4][NH:3][C:6]1[C:19]2[C:18](=[O:20])[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[C:11](=[O:21])[C:10]=2[CH:9]=[CH:8][CH:7]=1Participants
3
Procedure
The hydrazine may be added gradually or all at once. If the hydrazine is gradually added, intermediate reduction steps of the nitroanthraquinone employed, e.g. hydroxylaminoanthraquinone, may be isolated. The nitroanthraquinone used is preferably reacted directly to the amino step. The resulting amino compound may be isolated from the reaction mixture by methods known per se.
Sources & evidence
- ORD record
- ord-6e6a4220dda547669cfe61ff3d0754d3
- Source dataset
- uspto-grants-1977_04
- Patent number
- US04016182
Reaction notes
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