Potassium Iodide → HCID 13090791, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[N:4][C:5]2[C:10]([CH:11]=1)=[CH:9][CH:8]=[C:7]([Cl:12])[C:6]=2[CH2:13]Cl.[C-]#N.[K+].[I-].[K+].[CH3:20][N:21](C)C=O>O>[Cl:1][C:2]1[CH:3]=[N:4][C:5]2[C:10]([CH:11]=1)=[CH:9][CH:8]=[C:7]([Cl:12])[C:6]=2[CH2:13][C:20]#[N:21]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
49 parts of 3,7-dichloro-8-chloromethylquinoline (Example 1), 13 parts of potassium cyanide and 0.1 part of potassium iodide in 300 parts of dimethylformamide were heated at 150° C. for 4 hours. Water was added to the reaction solution and the precipitated product was filtered off with suction and recrystallized from methylglycol. 32 parts of 3,7-dichloro-8-cyanomethylquinoline of melting point 152° C. were obtained. The yield corresponds to 67% of theory.
Workup
- filtrationthe precipitated product was filtered off with suction
- customrecrystallized from methylglycol
Sources & evidence
- ORD record
- ord-d4d9b9e65f8b456ebb1a61abe9d2ae5c
- Source dataset
- uspto-grants-1985_02
- Patent number
- US04497651
Reaction notes
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