Hydrochloric Acid → HCID 20406529, compound
Reaction equation
Cl.[CH3:2][NH:3][C:4](=[O:18])[N:5]([C:9]1[S:10][C:11]([C:14]([F:17])([F:16])[F:15])=[N:12][N:13]=1)[N:6]=CC>O>[CH3:2][NH:3][C:4](=[O:18])[N:5]([C:9]1[S:10][C:11]([C:14]([F:15])([F:16])[F:17])=[N:12][N:13]=1)[NH2:6]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Concentrated hydrochloric acid (1.0 ml) was added to a stirred suspension of acetaldehyde 4-methyl-2-(5-trifluoromethyl-1,3,4-thiadiazol-2-yl)semicarbazone in water (200 ml). The mixture was stirred at room temperature for 3 days, and was filtered. The solid was dried and crystallised from ethyl acetate to give 4-methyl-2-(5-trifluoromethyl-1,3,4-thiadiazol-2-yl)semicarbazide (10.0 g) as a white solid, mp 181°-182° C.
Workup
- filtrationwas filtered
- customThe solid was dried
- customcrystallised from ethyl acetate
Sources & evidence
- ORD record
- ord-a46e116cf16c4332b99f5ff40504d8a2
- Source dataset
- uspto-grants-1985_02
- Patent number
- US04501605
Reaction notes
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