Potassium Hydroxide → HCID 13882135, compound
Reaction equation
[Cl:1][C:2]1[C:7]([Cl:8])=[CH:6][CH:5]=[CH:4][C:3]=1[N:9]1[C:13]([C:14]#[N:15])=[C:12]([C:16]([O:18]CC)=[O:17])[CH:11]=[N:10]1.[OH-:21].[K+]>C(O)C>[C:16]([C:12]1[CH:11]=[N:10][N:9]([C:3]2[CH:4]=[CH:5][CH:6]=[C:7]([Cl:8])[C:2]=2[Cl:1])[C:13]=1[C:14]([NH2:15])=[O:21])([OH:18])=[O:17]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A 15 g. portion of ethyl 1-(2,3-dichlorophenyl)-5-cyano-4-pyrazolecarboxylate was stirred under reflux overnight in 200 ml. of ethanol with 6 g. of potassium hydroxide. The reaction mixture was chromatographed over silica gel, and the product-containing fractions were combined and evaporated to dryness. The residues were recrystallized from ethanol-water to obtain 1.31 g. of the desired product, m.p. 228°-230°, which was identified by elemental analysis.
Workup
- temperatureunder reflux overnight in 200 ml
- customThe reaction mixture was chromatographed over silica gel
- customevaporated to dryness
- customThe residues were recrystallized from ethanol-water
- customto obtain 1.31 g
Sources & evidence
- ORD record
- ord-c6dec9ada87f4a4aad1b24d042a83d0e
- Source dataset
- uspto-grants-1988_10
- Patent number
- US04775409
Reaction notes
Loading…