Water → HCID 73068188, compound
Reaction equation
[Cl:1][C:2]1[CH:23]=[C:22]([O:24][CH2:25][CH:26]=[C:27]([Cl:29])[Cl:28])[CH:21]=[C:20]([Cl:30])[C:3]=1[O:4][CH2:5][CH2:6][CH2:7][O:8][C:9]1[CH:10]=[C:11]2[C:16](=[CH:17][CH:18]=1)[C:15](=O)[CH2:14][CH2:13][CH2:12]2.C([O-])(=O)C.[Na+].Cl.[CH3:37][O:38][NH2:39].O>C(O)C>[CH3:37][O:38][N:39]=[C:15]1[C:16]2[C:11](=[CH:10][C:9]([O:8][CH2:7][CH2:6][CH2:5][O:4][C:3]3[C:2]([Cl:1])=[CH:23][C:22]([O:24][CH2:25][CH:26]=[C:27]([Cl:28])[Cl:29])=[CH:21][C:20]=3[Cl:30])=[CH:18][CH:17]=2)[CH2:12][CH2:13][CH2:14]1Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
1.24 g of 6-{3-[2,6-dichloro-4-(3,3-dichloro-allyloxy)-phenoxy]-propoxy}-3,4-dihydro-2H-naphthalen-1-one, 0.23 g of sodium acetate and 0.23 g of O-methylhydroxylamine hydrochloride are stirred in 10 ml of ethanol at 50° C. for 18 hours. The reaction mixture is poured into water and extracted with ethyl acetate. After concentration of the organic phases and purification over silica gel, the title compound is obtained. M.p. 75-77° C.
Workup
- extractionextracted with ethyl acetate
- customAfter concentration of the organic phases and purification over silica gel
Sources & evidence
- ORD record
- ord-89b045d842854837b44b54b46ba807e7
- Source dataset
- uspto-grants-2009_08
- Patent number
- US07569727B2
Reaction notes
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