Hydrogen Peroxide → HCID 21555251, compound
Reaction equation
[OH:1][C:2]1[CH2:7][C:6]([CH3:9])([CH3:8])[CH2:5][C:4](=[O:10])[C:3]=1[S:11][CH2:12][CH2:13][CH:14]([CH3:16])[CH3:15].[OH:17]O>C(O)(=O)C>[OH:10][C:4]1[CH2:5][C:6]([CH3:8])([CH3:9])[CH2:7][C:2](=[O:1])[C:3]=1[S:11]([CH2:12][CH2:13][CH:14]([CH3:16])[CH3:15])=[O:17]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 3-hydroxy-2-isopentylthio-5,5-dimethyl-2-cyclohexen-1-one (10 g., 0.041 mole), 30 percent hydrogen peroxide (4.7 g., 0.041 mole), and 100 ml. of glacial acetic acid was allowed to stand at room temperature for 24 hours. The mixture was poured into ice water and the precipitated pink crystals were filtered and dried (9.1 g., m.p. 64.5°-66°C.).
Workup
- filtrationthe precipitated pink crystals were filtered
- customdried (9.1 g., m.p. 64.5°-66°C.)
Sources & evidence
- ORD record
- ord-0b6b35c775154489b36b7df1240ed732
- Source dataset
- uspto-grants-1976_03
- Patent number
- US03943176
Reaction notes
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