2,4-Dinitrotoluene → 2,3-Dinitrotoluene
Reaction equation
[N+:1]([O-:4])([O-:3])=O.[NH4+].[N+:6]([C:9]1[CH:14]=[C:13]([N+]([O-])=O)[CH:12]=[CH:11][C:10]=1[CH3:18])([O-:8])=[O:7].[N+](C1C=CC=C([N+]([O-])=O)C=1C)([O-])=O.[Al]>>[N+:1]([C:14]1[C:9]([N+:6]([O-:8])=[O:7])=[C:10]([CH3:18])[CH:11]=[CH:12][CH:13]=1)([O-:4])=[O:3]Participants
5
Conditions
- Temperature
- 70 °C
Procedure
Eighty-five (85) parts of porous prill ammonium nitrate (average particle size, 1.7 mm; oil absorbency, 17%) preheated to 70° C., and 14 parts of a liquid dinitrotoluene mixture which was prepared by mixing 2,4-dinitrotoluene with 2,6-dinitrotoluene and heating at 70° C. were thoroughly mixed using a horizontal kneader equipped with a sigma wing, thereby obtaining a granular explosive of the present invention. After cooling, the granular explosive and 1 part of flake-shaped aluminium (P-0100; manufactured by Toyo Aluminium) were mixed using a horizontal kneader. The thus obtained explosive was recovered from the kneader and packed in a paper shell.
Workup
- custompreheated to 70° C.
- additionwere thoroughly mixed
- customequipped with a sigma wing
- customobtaining a granular explosive of the present invention
- temperatureAfter cooling
- customThe thus obtained explosive was recovered from the kneader
Sources & evidence
- ORD record
- ord-8993242e9b314d44b75cb6dad7de657b
- Source dataset
- uspto-grants-1997_10
- Patent number
- US05675119
Reaction notes
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