Acetone → HCID 13014066, compound
Reaction equation
[CH3:1][C:2]([CH3:4])=O.[NH:5]([C:7]1[S:11][N:10]=[C:9]([C:12]([Cl:15])([Cl:14])[Cl:13])[N:8]=1)[NH2:6]>>[Cl:15][C:12]([Cl:13])([Cl:14])[C:9]1[N:8]=[C:7]([NH:5][N:6]=[C:2]([CH3:4])[CH3:1])[S:11][N:10]=1Participants
3
Procedure
A mixture of 5 ml (3.9 g, 0.068 mole) acetone and 2.4 g (0.01 mole) 5-hydrazino-3-trichloromethyl-1,2,4-thiadiazole was heated 0.5 hour on a steam bath. The solid that was left after evaporation of the excess acetone was recrystallized from ligroin to yield 0.95 g (mp. 75°-77° C.). A second crop of 1.2 g (mp. 66° C.) was obtained after concentration of the solvent. Total yield was 2.15 g (79% yield).
Workup
- temperaturewas heated 0.5 hour on a steam bath
- waitThe solid that was left
- customafter evaporation of the excess acetone
- customwas recrystallized from ligroin
- customto yield 0.95 g (mp. 75°-77° C.)
- customA second crop of 1.2 g (mp. 66° C.) was obtained after concentration of the solvent
Sources & evidence
- ORD record
- ord-fc9a249ee6e84b8a957b2ac740c23cbb
- Source dataset
- uspto-grants-1981_04
- Patent number
- US04263312
Reaction notes
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