Ethanol → HCID 178463174、化合物
反応式
[OH:1][C:2]1[N:3]=[N:4][C:5]([OH:10])=[C:6]([Cl:9])[C:7]=1[Cl:8].[OH-].[Na+].[CH2:13](I)[CH3:14].C(O)C>C1C=CC=CC=1.O>[CH2:13]([N:3]1[C:2](=[O:1])[C:7]([Cl:8])=[C:6]([Cl:9])[C:5]([OH:10])=[N:4]1)[CH3:14][OH:1][C:2]1[N:3]=[N:4][C:5]([OH:10])=[C:6]([Cl:9])[C:7]=1[Cl:8].[OH-].[Na+].[CH2:13](I)[CH3:14].C(O)C>C1C=CC=CC=1.O>[CH2:13]([N:3]1[C:2](=[O:1])[C:7]([Cl:8])=[C:6]([Cl:9])[C:5]([OH:10])=[N:4]1)[CH3:14]A mixture comprising 5.00 g of 3,6-dihydroxy-4,5-dichloropyridazine, 2.21 g of sodium hydroxide, 5.60 g of ethyl iodide, 40 ml of ethanol and water, was stirred at a temperature of from 60° to 70° C. for 4 hours. Most ethanol was distilled off under reduced pressure. Then, dilute hydrochrolic acid and chloroform were added to the residue, and the mixture was vigorously shaked. The chloroform layer was separated and washed with water, followed by drying over sodium sulfate. Then, the solvent was distilled off to obtain a light orange solid substance. The solid substance was treated with benzene to obtain 3.56 g of the above identified compound as colorless crystals.
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