3-(4-Methylphenoxy)-2,2-dimethylcyclopropanecarboxylic acid → alpha-Cyano-4-fluoro-3-phenoxybenzyl 3-(4-methylphenoxy)-2,2-dimethylcyclopropanecarboxylate

HRID 28098Notes

Reaction equation

HRID 28098 reaction equation
[CH3:1][C:2]1[CH:16]=[CH:15][C:5]([O:6][CH:7]2[CH:9]([C:10]([OH:12])=[O:11])[C:8]2([CH3:14])[CH3:13])=[CH:4][CH:3]=1.CS(O[CH:22]([C:37]#[N:38])[C:23]1[CH:28]=[CH:27][C:26]([F:29])=[C:25]([O:30][C:31]2[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=2)[CH:24]=1)(=O)=O>>[CH3:1][C:2]1[CH:16]=[CH:15][C:5]([O:6][CH:7]2[CH:9]([C:10]([O:12][CH:22]([C:37]#[N:38])[C:23]3[CH:28]=[CH:27][C:26]([F:29])=[C:25]([O:30][C:31]4[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=4)[CH:24]=3)=[O:11])[C:8]2([CH3:14])[CH3:13])=[CH:4][CH:3]=1

Participants

3

Procedure

Following the procedure of Example 2, 3-(4-methylphenoxy)-2,2-dimethylcyclopropanecarboxylic acid is reacted with α-cyano-4-fluoro-3-phenoxybenzyl methanesulfonate to yield α-cyano-4-fluoro-3-phenoxybenzyl 3-(4-methylphenoxy)-2,2-dimethylcyclopropanecarboxylate.

Sources & evidence

ORD record
ord-28df55b17e2546d7b3a38436ad3ceb05
Source dataset
uspto-grants-1980_09
Patent number
US04225533

Reaction notes

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