Water → HCID 86602674, compound
Reaction equation
[Cl:1][C:2]1[CH:16]=[C:15]([O:17][CH2:18][CH:19]=[C:20]([Cl:22])[Cl:21])[CH:14]=[C:13]([Cl:23])[C:3]=1[O:4][CH2:5][CH2:6][CH2:7][O:8]S(C)(=O)=O.C(=O)([O-])[O-].[K+].[K+].O[C:31]1[CH:36]=[CH:35][C:34]([C:37](=[O:41])[CH2:38][O:39][CH3:40])=[CH:33][CH:32]=1.O>CN(C)C=O>[Cl:1][C:2]1[CH:16]=[C:15]([O:17][CH2:18][CH:19]=[C:20]([Cl:22])[Cl:21])[CH:14]=[C:13]([Cl:23])[C:3]=1[O:4][CH2:5][CH2:6][CH2:7][O:8][C:31]1[CH:36]=[CH:35][C:34]([C:37](=[O:41])[CH2:38][O:39][CH3:40])=[CH:33][CH:32]=1Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
1.8 g of methanesulfonic acid 3-[2,6-dichloro-4-(3,3-dichloro-allyloxy)-phenoxy]-propyl ester, 1.8 g of potassium carbonate and 1.97 g of 1-(4-hydroxy-phenyl)-2-methoxyethanone are stirred in 30 ml of dimethylformamide at 50° C. for 17 hours. The reaction mixture is poured into water and extracted with ethyl acetate. After concentration of the organic phases and purification over silica gel, 1-(4-{3-[2,6-dichloro-4-(3,3-dichloro-allyloxy)-phenoxy]-propoxy}-phenyl)-2-methoxy-ethanone is obtained.
Workup
- extractionextracted with ethyl acetate
- customAfter concentration of the organic phases and purification over silica gel
Sources & evidence
- ORD record
- ord-d1f156a5651c4f42bbec5ce8f21b0611
- Source dataset
- uspto-grants-2009_08
- Patent number
- US07569727B2
Reaction notes
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