Reaktion #317767
ord-7919c91fd68a426cb45669c1a7f2747c
Reaktionsgleichung
Edukte
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1SonstigeIt was quenched with water
- 2Filtrationthe resulting white precipitate was filtered off
- 3SonstigeThe filtrate was partitioned between ethyl acetate and water
- 4TrocknenThe organic layer was dried over sodium sulfate
- 5Einengenconcentrated in vacuo
- 6SonstigeThe crude material was purified by silica gel column chromatography
- 7Wascheneluting with hexane/ethyl acetate (4:1)
- 8SonstigeThe yellow oil obtained
- 9Sonstigequenched with methanol
- 10workup.STIRRINGIt was stirred at room temperature for 1 hour
- 11Einengenconcentrated in vacuo
Vorschrift
To a solution of titanium(IV) ethoxide (1.32 g, 5.8 mol) and N-(4-acetyl-2-methylphenyl) methanesulfonamide (800 mg, 3.5 mmol) in tetrahydrofuran (20 mL) was added (R)-(+)-2-methyl-2-propanesulfinamide (423 mg, 350 mmol) under a nitrogen atmosphere and the mixture was heated at 70° C. for 16 hours. It was quenched with water and the resulting white precipitate was filtered off. The filtrate was partitioned between ethyl acetate and water. The organic layer was dried over sodium sulfate and concentrated in vacuo. The crude material was purified by silica gel column chromatography, eluting with hexane/ethyl acetate (4:1). The yellow oil obtained was dissolved in tetrahydrofuran (10 mL) and the solution was added to sodium borohydride (242 mg, 6.4 mmol) in tetrahydrofuran (10 mL) at −70° C. The mixture was stirred at −70° C. for 5 hours and then quenched with methanol. It was stirred at room temperature for 1 hour and concentrated in vacuo to furnish 530 mg (45%) of the title compound. MS (ESI) m/z 333 (M+H)+, 331 (M−H)−.