Hydrochloric Acid → HCID 13742395, compound
Reaction equation
CN(C)C=[N:4][C:5]1[S:6][C:7]([N+:13]([O-:15])=[O:14])=[C:8]([Cl:12])[C:9]=1[C:10]#[N:11].Cl>C(O)C>[NH2:4][C:5]1[S:6][C:7]([N+:13]([O-:15])=[O:14])=[C:8]([Cl:12])[C:9]=1[C:10]#[N:11]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 5.2 parts of N,N-dimethyl-N'-(4-chloro-3-cyano-5-nitrothien-2-yl)-formamidine, 50 parts of ethanol and 5 parts of concentrated hydrochloric acid is heated at the boil for 3 hours and then poured onto ice water. The precipitate is filtered off under suction, washed with water and dried. 3.2 parts (79% of theory) of 2-amino-4-chloro-3-cyano-5-nitrothiophene are obtained. Decomposition temperature: 227° C. (from o-dichlorobenzene).
Workup
- temperatureis heated at the boil for 3 hours
- additionpoured onto ice water
- filtrationThe precipitate is filtered off under suction
- washwashed with water
- customdried
Sources & evidence
- ORD record
- ord-a7f6f9373dcd4264b907013ff5a7506f
- Source dataset
- uspto-grants-1993_04
- Patent number
- US05206375
Reaction notes
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