(4-(Allyloxy)-5-bromo-2-chlorophenyl)(4-ethylphenyl)methanone → (3-(Allyloxy)-5-bromo-2-chlorophenyl)(4-methoxyphenyl)methanone

HRID 2206771Notes

Reaction equation

HRID 2206771 reaction equation
[CH2:1]([O:4][C:5]1[C:10](Br)=[CH:9][C:8](C(C2C=CC(CC)=CC=2)=O)=[C:7](Cl)[CH:6]=1)C=C.[CH2:23]([O:26][C:27]1[C:28]([Cl:40])=[C:29]([CH:36]=[C:37]([Br:39])[CH:38]=1)[C:30](N(OC)C)=[O:31])[CH:24]=[CH2:25]>>[CH2:23]([O:26][C:27]1[C:28]([Cl:40])=[C:29]([C:30]([C:8]2[CH:9]=[CH:10][C:5]([O:4][CH3:1])=[CH:6][CH:7]=2)=[O:31])[CH:36]=[C:37]([Br:39])[CH:38]=1)[CH:24]=[CH2:25]

Participants

3

Reactant 2

HCID 86714031(4-(Allyloxy)-5-bromo-2-chlorophenyl)(4-ethylphenyl)methanoneHCID 892838625-bromo-2-chloro-N-methoxy-N-methyl-3-prop-2-enoxybenzamide

Product 1

HCID 89283863(3-(Allyloxy)-5-bromo-2-chlorophenyl)(4-methoxyphenyl)methanone

Procedure

Similar procedure with preparation of 31 proceeded except for using compound 182 to obtain the compound 183.

Sources & evidence

ORD record
ord-dd72eb21f33045dfacc063f644af8ab4
Source dataset
uspto-grants-2016_06
Patent number
US09371303B2

Reaction notes

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