Reaction equation
[CH3:1][S:2][C:3]1[CH:8]=[CH:7][C:6]([N+:9]([O-:11])=[O:10])=[CH:5][CH:4]=1.I(O)(=O)(=O)=[O:13].S([O-])([O-])(=O)=S.[Na+].[Na+]>C(#N)C.[Fe](Cl)(Cl)Cl>[CH3:1][S:2]([C:3]1[CH:4]=[CH:5][C:6]([N+:9]([O-:11])=[O:10])=[CH:7][CH:8]=1)=[O:13]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
A suspension of 25.0 g (147.8 mmol) 1-methylsulfanyl-4-nitro-benzene and 0.69 g (4.2 mmol) iron(III) chloride (anhydrous) in 120 ml acetonitrile is treated with 36.0 g (158.1 mmol) periodic acid and stirred at room temperature. At the start of heat evolution, the mixture is transiently cooled with an ice-bath, so that the temperature does not rise above 30° C. After the heat evolution has subsided, the mixture is stirred at room temperature for a further 10 mins. The mixture is poured into a solution of 150 g sodium thiosulphate in 1000 ml ice-water and then extracted with DCM. The combined organic phases are washed with saturated NaCl solution, dried (Na2SO4), filtered and concentrated. The remaining residue is recrystallised from toluene. 23.6 g (128.0 mmol, corresponding to 86% of theor.) of the product is obtained.
Workup
- temperatureAt the start of heat evolution, the mixture is transiently cooled with an ice-bath, so that the temperature
- customdoes not rise above 30° C
- stirringthe mixture is stirred at room temperature for a further 10 mins
- extractionextracted with DCM
- washThe combined organic phases are washed with saturated NaCl solution
- dry with materialdried (Na2SO4)
- filtrationfiltered
- concentrationconcentrated
- customThe remaining residue is recrystallised from toluene
- custom23.6 g (128.0 mmol, corresponding to 86% of theor.) of the product is obtained
Sources & evidence
- ORD record
- ord-cafb6242f564439da553abac38a251f3
- Source dataset
- uspto-grants-2013_09
- Patent number
- US08524724B2
Linked notes
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