Ethyl oxoacetate → HCID 86757434, compound

HRID 1597432Notes

Reaction equation

HRID 1597432 reaction equation
[C:1]([O:5][CH2:6][CH3:7])(=[O:4])[CH:2]=O.[CH3:8][S:9]([C:12]1[CH:17]=[CH:16][C:15]([O:18][C:19]2[CH:24]=[CH:23][C:22]([O:25][C:26]([F:29])([F:28])[F:27])=[CH:21][CH:20]=2)=[CH:14][CH:13]=1)(=[O:11])=[O:10]>>[F:29][C:26]([F:27])([F:28])[O:25][C:22]1[CH:23]=[CH:24][C:19]([O:18][C:15]2[CH:14]=[CH:13][C:12]([S:9](/[CH:8]=[CH:2]/[C:1]([O:5][CH2:6][CH3:7])=[O:4])(=[O:11])=[O:10])=[CH:17][CH:16]=2)=[CH:20][CH:21]=1

Participants

3

Reactant 2

HCID 70211Ethyl oxoacetateHCID 102866141-(Methanesulfonyl)-4-[4-(trifluoromethoxy)phenoxy]benzene

Product 1

HCID 86757434HCID 86757434, compound

Procedure

The title compound was prepared from ethyl glyoxalate and 4-(4′-trifluoromethoxyphenyloxy)-phenyl methyl sulfone following the procedures of Examples 126A, 126B and 75B.

Sources & evidence

ORD record
ord-0d34131cd917404b8a79bf0e1f023a7a
Source dataset
uspto-grants-2001_09
Patent number
US06294573B1

Reaction notes

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