Methanol → Methyl phenyl sulfoxide

A solution of thioanisole (2.48 g, 20 mmol) in methanol (100 mL) in a 250-mL flask was cooled in an ice bath. Stabilized BrCl solution (15 wt. % solution, 18 mL, ~28 mmol) was then added dropwise, with stirring. After the addition, the ice bath was removed, the reaction mixture was allowed to stand at room temperature and the progress of the reaction was monitored by gas chromatography (GC). In less than one hour, the starting material was totally converted to product and the orange-reddish solution turned light yellow. The reaction mixture was quenched with a few drops of sodium sulfite solution, diluted with ethylene dichloride (EDC, 100 mL), and washed with water (100 mL). After phase separation, the colorless organic layer was dried (Na2SO4) and concentrated under reduced pressure to furnish 2.44 g (~87% yield) of methyl phenyl sulfoxide as a colorless oil. GC analysis indicated the presence of ~2% of the corresponding sulfone.

1. additionAfter the addition
2. customthe ice bath was removed
3. customto stand at room temperature
4. waitIn less than one hour
5. customThe reaction mixture was quenched with a few drops of sodium sulfite solution
6. additiondiluted with ethylene dichloride (EDC, 100 mL)
7. washwashed with water (100 mL)
8. customAfter phase separation
9. dry with materialthe colorless organic layer was dried (Na2SO4)
10. concentrationconcentrated under reduced pressure

ORD record

ord-f84a4a6aa7bc4e8ebdfb7e5bbf678550

Source dataset

uspto-grants-1999_05

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05900512