P-Cresol → HCID 15585792, compound

HRID 2049828Notes

Reaction equation

HRID 2049828 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.C1C(O)=CC=C(C)C=1.CS(O[CH:30]([C:44]#[N:45])[C:31]1[CH:36]=[CH:35][CH:34]=[C:33]([O:37][C:38]2[CH:43]=[CH:42][CH:41]=[CH:40][CH:39]=2)[CH:32]=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:30]([C:44]#[N:45])[C:31]3[CH:36]=[CH:35][CH:34]=[C:33]([O:37][C:38]4[CH:39]=[CH:40][CH:41]=[CH:42][CH:43]=4)[CH:32]=3)=[O:11])[C:8]2([CH3:14])[CH3:13])=[CH:4][CH:3]=1

Participants

4

Reactant 3

HCID 2879P-CresolHCID 204545163-(4-Methylphenoxy)-2,2-dimethylcyclopropanecarboxylic acidHCID 20482835alpha-Cyano-m-phenoxybenzyl mesylate

Product 1

HCID 15585792HCID 15585792, compound

Procedure

Following the procedure of Example 2, 3-(4-methylphenoxy)-2,2-dimethylcyclopropanecarboxylic acid is prepared from 4-cresol, which is then reacted with α-cyano-m-phenoxybezyl methanesulfonate to yield α-cyano-m-phenoxybezyl 3-(4-methylphenoxy)-2,2-dimethylcyclopropanecarboxylate.

Sources & evidence

ORD record
ord-f2986745ca7944608f2e1fec1306b3f6
Source dataset
uspto-grants-1980_04
Patent number
US04198527

Reaction notes

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