Water → HCID 18784870, compound
Reaction equation
[OH:1]OS([O-])=O.[K+].[CH3:7][O:8][C:9]1[C:17]2[O:16][C:15]([S:18][CH3:19])=[CH:14][C:13]=2[CH:12]=[CH:11][CH:10]=1.[OH2:20]>>[CH3:19][S:18]([C:15]1[O:16][C:17]2[C:9]([O:8][CH3:7])=[CH:10][CH:11]=[CH:12][C:13]=2[CH:14]=1)(=[O:1])=[O:20]Participants
4
Procedure
A solution of Oxone® (7.37 g) in water (40 ml) was added to a solution of 7-methoxy-2-methylsulfanylbenzofuran (2.24 g) and the reaction mixture was stirred at room temperature overnight. The methanol was removed in vacuo and the resulting slurry was extracted with ethyl acetate (2×200 ml). The combined organic phases were washed with brine (200 ml) and then dried over sodium sulfate. The solvent was removed in vacuo to furnish the title compound as a yellow solid (2.24 g).
Workup
- customThe methanol was removed in vacuo
- extractionthe resulting slurry was extracted with ethyl acetate (2×200 ml)
- washThe combined organic phases were washed with brine (200 ml)
- dry with materialdried over sodium sulfate
- customThe solvent was removed in vacuo
Sources & evidence
- ORD record
- ord-39ba42ff805349f483983f04bf9a52f1
- Source dataset
- uspto-grants-2000_05
- Patent number
- US06066657
Reaction notes
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