HCID 42629602, compound → HCID 87559971, compound

HRID 1960100Notes

Reaction equation

HRID 1960100 reaction equation
C[O:2][C:3](=O)/[C:4](/[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[CH2:14][O:15][C:16]1[CH:21]=[CH:20][C:19]([CH:22]=[C:23]([Cl:25])[Cl:24])=[CH:18][C:17]=1[CH3:26])=[N:5]/[O:6][CH3:7].COC(=O)/[C:31](/C1C=CC=CC=1COC1C=CC(C=C(Cl)Cl)=CC=1Cl)=[N:32]/OC>>[Cl:24][C:23]([Cl:25])=[CH:22][C:19]1[CH:20]=[CH:21][C:16]([O:15][CH2:14][C:9]2[CH:10]=[CH:11][CH:12]=[CH:13][C:8]=2/[C:4](=[N:5]\[O:6][CH3:7])/[C:3]([NH:32][CH3:31])=[O:2])=[C:17]([CH3:26])[CH:18]=1

Participants

3

Reactant 2

HCID 42629602HCID 42629602, compoundHCID 87558880HCID 87558880, compound

Product 1

HCID 87559971HCID 87559971, compoundYield 86%

Procedure

The procedure of Example 40 was repeated except for using methyl-(E)-2-(2-((4-(2,2-dichlorovinyl)-2-methylphenoxy)methyl)phenyl)-2-methoxyiminoacetate (0.408 g, 1 mmol) obtained in Example 41 instead methyl-(E)-2-(2-((2-chloro-4-(2,2-dichlorovinyl)phenoxy)methyl)phenyl)-2-methoxyiminoacetate to obtain the title compound (0.350 g, 86%).

Sources & evidence

ORD record
ord-87749eafa3dd4730bff9813307c02070
Source dataset
uspto-grants-2013_04
Patent number
US08410302B2

Reaction notes

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