Methanol → HCID 53810175, compound
Reaction equation
[NH4+].[Cl:2][C:3]1[C:4]([C:15]#[N:16])=[C:5]([C:9]([Cl:14])=[C:10](Cl)[C:11]=1[Cl:12])[C:6]([O-:8])=[O:7].[CH3:17][O-:18].[Na+].[CH3:20]O>CN(C)C=O>[CH3:20][O:8][C:6](=[O:7])[C:5]1[C:9]([Cl:14])=[C:10]([O:18][CH3:17])[C:11]([Cl:12])=[C:3]([Cl:2])[C:4]=1[C:15]#[N:16]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
30.2 g of 3,4,5,6-tetrachloro-2-cyanobenzoic acid ammonium salt is introduced, with stirring, into a solution of 10.8 g of sodium methylate in 32 ml of methanol and 100 ml of dimethylformamide. After the slightly exothermic reaction has subsided, stirring is continued for 15 hours at room temperature.
Workup
- customAfter the slightly exothermic reaction
Sources & evidence
- ORD record
- ord-c659ce3cc6324289a4f266c4722a0ad2
- Source dataset
- uspto-grants-1977_10
- Patent number
- US04052410
Reaction notes
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