HCID 85773171, compound → HCID 25070766, compound
Reaction equation
[CH:1]([C:4]1[CH:5]=[C:6]([S:14][C:15]([S:18][C:19]2[CH:24]=[C:23]([CH:25]([CH3:27])[CH3:26])[C:22]([OH:28])=[C:21]([CH:29]([CH3:31])[CH3:30])[CH:20]=2)([CH3:17])[CH3:16])[CH:7]=[C:8]([CH:11]([CH3:13])[CH3:12])[C:9]=1[OH:10])([CH3:3])[CH3:2]>ClCCl.CCCCCC.[O-2].[O-2].[Mn+4]>[CH3:17][C:15]1([CH3:16])[S:14][C:6]2([CH:5]=[C:4]([CH:1]([CH3:3])[CH3:2])[C:9](=[O:10])[C:8]([CH:11]([CH3:12])[CH3:13])=[CH:7]2)[C:19]2([CH:24]=[C:23]([CH:25]([CH3:27])[CH3:26])[C:22](=[O:28])[C:21]([CH:29]([CH3:31])[CH3:30])=[CH:20]2)[S:18]1Participants
5
Reactant 1
Product 1
Reagents, catalysts & solvents 3
Procedure
To a mixed solution of 2,2-bis(3,5-diisopropyl-4-hydroxyphenylthio)propane (500 mg, 1.09 mmol) in dichloromethane (5 mL) and hexane (5 mL) was added manganese dioxide (500 mg). The mixture was stirred for 4 hours and then filtered by using a celite, and the resulting filtrate was concentrated. Hexane was added to the residue, and the mixture was stored in a refrigerator. The generated solid was separated by a filtration, washed with hexane, and then dried to synthesize an, objective compound.
Workup
- filtrationfiltered
- concentrationthe resulting filtrate was concentrated
- additionHexane was added to the residue
- customThe generated solid was separated by a filtration
- washwashed with hexane
- customdried
- customto synthesize an, objective compound
Sources & evidence
- ORD record
- ord-3f619134f95b43a4af27bf39b45efb72
- Source dataset
- uspto-grants-2012_02
- Patent number
- US08119686B2
Reaction notes
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