Hydrogen Peroxide → 1-[2-(2,6-Diethyl-4-methylphenyl)-2-oxoacetyl]-1-methyl-2-(1-methylsulfinyl-2-propylidene)hydrazine

HRID 579241Notes

Reaction equation

HRID 579241 reaction equation
[CH2:1]([C:3]1[CH:8]=[C:7]([CH3:9])[CH:6]=[C:5]([CH2:10][CH3:11])[C:4]=1[C:12](=[O:23])[C:13]([N:15]([CH3:22])[N:16]=[C:17]([CH3:21])[CH2:18][S:19][CH3:20])=[O:14])[CH3:2].[OH:24]O>CO>[CH2:10]([C:5]1[CH:6]=[C:7]([CH3:9])[CH:8]=[C:3]([CH2:1][CH3:2])[C:4]=1[C:12](=[O:23])[C:13]([N:15]([CH3:22])[N:16]=[C:17]([CH3:21])[CH2:18][S:19]([CH3:20])=[O:24])=[O:14])[CH3:11]

Participants

4

Procedure

To a 50 ml volume three-necked flask, 1-[2-(2,6-diethyl-4-methylphenyl)-2-oxoacetyl]-1-methyl-2-(1-methylsulfanyl-2-propylidene)hydrazine ((4-4)-(1)-39) (5.60 g) and methanol (14 ml) were added, and cooled on ice-bath. 33% of aqueous hydrogen peroxide solution (2.1 g) was added dropwise thereto. Then, the mixture was stirred at room temperature for 12 hours. The reaction mixture was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography (ethyl acetate to chloroform) to give 1.95 g of 1-[2-(2,6-diethyl-4-methylphenyl)-2-oxoacetyl]-1-methyl-2-(1-methylsulfinyl-2-propylidene)hydrazine ((4-19)-(1)-39).

Workup

  1. temperaturecooled on ice-bath
  2. concentrationThe reaction mixture was concentrated under reduced pressure

Sources & evidence

ORD record
ord-7f0bc63103384b76ac52ddc781bf376b
Source dataset
uspto-grants-2015_05
Patent number
US09040709B2

Reaction notes

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