Nitric Acid → 1,1,3,5,5,7-Hexanitro-3,7-diazacyclooctane
Reaction equation
[N+:1]([C:4]1([N+:20]([O-:22])=[O:21])[CH2:11][NH:10][CH2:9][C:8]([N+:15]([O-:17])=[O:16])([N+:12]([O-:14])=[O:13])[CH2:7][N:6]([N:18]=[O:19])[CH2:5]1)([O-:3])=[O:2].S(=O)(=O)(O)[OH:24].[N+:28]([O-])([OH:30])=[O:29]>>[N+:18]([N:6]1[CH2:7][C:8]([N+:15]([O-:17])=[O:16])([N+:12]([O-:14])=[O:13])[CH2:9][N:10]([N+:28]([O-:30])=[O:29])[CH2:11][C:4]([N+:1]([O-:3])=[O:2])([N+:20]([O-:22])=[O:21])[CH2:5]1)([O-:24])=[O:19]Participants
4
Procedure
nitrating the 3,3,7,7-tetranitro-1-nitrosoperhydro-1,5-diazocine in a mixture of concentrated sulfuric acid and 90% nitric acid at a temperature of from about 0° C. to about 5° C. to form 1,3,3,5,7,7-hexanitroperhydro-1,5-diazocine; and
Sources & evidence
- ORD record
- ord-9043644e562241f6b64386cc9cc03c3d