Methanol → HCID 76696795, compound
Reaction equation
[Cl:1][C:2]1[CH:22]=[C:21]([O:23][CH2:24][CH:25]=[C:26]([Cl:28])[Cl:27])[CH:20]=[C:19]([Cl:29])[C:3]=1[O:4][CH2:5][C:6](=[CH2:18])[CH2:7][O:8][C:9]1[CH:14]=[CH:13][C:12]([C:15](=O)[CH3:16])=[CH:11][CH:10]=1.Cl.[CH3:31][O:32][NH2:33].CO.C([O-])(=O)C.[Na+]>C(OCC)(=O)C>[CH3:31][O:32][N:33]=[C:15]([C:12]1[CH:11]=[CH:10][C:9]([O:8][CH2:7][C:6]([CH2:5][O:4][C:3]2[C:2]([Cl:1])=[CH:22][C:21]([O:23][CH2:24][CH:25]=[C:26]([Cl:27])[Cl:28])=[CH:20][C:19]=2[Cl:29])=[CH2:18])=[CH:14][CH:13]=1)[CH3:16]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 25 °C
Procedure
286 mg of 1-(4-{2-[2,6-dichloro-4-(3,3-dichloro-allyloxy)-phenoxymethyl]-allyloxy}-phenyl)-ethanone and 56 mg of O-methyl-hydroxylamine hydrochloride are introduced into 4 ml of methanol. 55 mg of sodium acetate are then added and the mixture is stirred for 24 hours at 25° C. The reaction mixture is diluted with 12 ml of ethyl acetate and washed twice with water. After concentration of the organic phase and purification over silica gel, the title compound is obtained.
Workup
- washwashed twice with water
- customAfter concentration of the organic phase and purification over silica gel
Sources & evidence
- ORD record
- ord-033f553136154cb5ab3f262b6d3d0ca3
- Source dataset
- uspto-grants-2009_12
- Patent number
- US07638514B2
Reaction notes
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