Hydrochloric Acid → p-Toluenesulfinic acid

Treat a solution of p-toluenesulfinic acid sodium salt, (6.0 g, 33.7 mmol) in H2O (20 mL) and tert-butyl methyl ether (10 mL) dropwise with concentrated HCl (3 mL) and stir for 10 minutes. Separate the solution in a separatory funnel and wash the organic layer with saturated aqueous sodium chloride. Dry the organic over Na2SO4, filter, and remove the solvent to afford 5.2 g (quantitative) of p-toluenesulfinic acid. Combine the acid with benzaldehyde (2.4 g, 22.5 mmol), formamide (3.8 g, 84.2 mmol), and trimethylsilylchloride (TMSCl) (4.0 g, 37.0 mmol) in 30 mL of a 1:1 solution of toluene/acetonitrile. Heat the reaction to 50° C. and stir for 5 hours. Cool the reaction and dilute in H2O (100 mL) and tert-butyl-methylether (TBME) (30 mL). Cool the solution in an ice bath, then filter to afford 4.5 g (70%) of desired product. Dry the solid under vacuum overnight to remove any residual water. 1H-NMR (DMSO): 9.75 (d, 1H), 7.98 (s, 1H), 7.69 (d, 21), 7.53 (d, 2H), 7.39 (m, 5H), 6.36 (d, 1H), 2.38 (s, 1H)

1. customSeparate the solution in a separatory funnel
2. washwash the organic layer with saturated aqueous sodium chloride
3. dry with materialDry the organic over Na2SO4
4. filtrationfilter
5. customremove the solvent

ORD record

ord-9be575e5108f46dc8d4eca85f848bcb0

Source dataset

uspto-grants-2008_01

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07320995B2