Ethyl chloroformate → HCID 135731743, compound
Reaction equation
[Cl:1][C:2]1[N:3]=[N:4][C:5]([C:8]2[CH:13]=[CH:12][C:11]([OH:14])=[CH:10][C:9]=2[OH:15])=[CH:6][CH:7]=1.Cl[C:17]([O:19][CH2:20][CH3:21])=[O:18]>N1C=CC=CC=1>[Cl:1][C:2]1[N:3]=[N:4][C:5]([C:8]2[CH:13]=[CH:12][C:11]([O:14][C:17]([O:19][CH2:20][CH3:21])=[O:18])=[CH:10][C:9]=2[OH:15])=[CH:6][CH:7]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
3-Chloro-6-(2,4-dihydroxyphenyl)pyridazine (1 mole) was treated with ethyl chloroformate (1.1 mole) in pyridine to give 3-chloro-6-(4-ethoxycarbonyloxy-2-hydroxyphenyl)pyridazine.
Sources & evidence
- ORD record
- ord-d84fecdb874b4373984308fe638e7863
- Source dataset
- uspto-grants-1978_09
- Patent number
- US04111935
Reaction notes
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