Reaktion #44478
ord-3e971a9c509847b5957a35ece801dc74
Reaktionsgleichung
Edukte
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1TemperaturThe reaction was cooled to 0° C.
- 2workup.STIRRINGstirred
- 3FiltrationThe reaction was filtered through a pad of celite
- 4Waschenrinsed with methanol
- 5Einengenconcentrated under vacuo
- 6Waschenwashed with water (25 mL)
- 7TrocknenThe organic layer was dried with MgSO4
- 8Filtrationfiltered
- 9Sonstigeevaporated in vacuo
- 10workup.STIRRINGstirred for three hours
- 11Waschenwashed with water (50 mL) and brine (25 mL)
- 12TrocknenThe organic layer was dried with MgSO4
- 13Filtrationfiltered
- 14Sonstigeevaporated in vacuo
- 15SonstigeThe crude product was purified by flash chromatography (hexanes:ethyl acetate 95:5 to 75:25)
Vorschrift
Sodium borohydride (0.213 g, 5.77 mmoles) was added to a solution of Example 1A (0.7 g, 2.92 mmoles) in methanol (3 mL) and tetrahydrofuran (3 mL) and stirred at 60° C. for two hours. The reaction was cooled to 0° C. and O-phosphoric acid (1.6 g, 17.4 mmoles) was added and stirred. The reaction was filtered through a pad of celite, rinsed with methanol, and concentrated under vacuo. The crude oil was taken up in ethyl acetate (25 mL) and washed with water (25 mL). The organic layer was dried with MgSO4, filtered and evaporated in vacuo. The resulting oil was taken up in N,N-dimethylformamide (4 mL) and imidazole (391 g, 5.76 mmoles) and Tert-butyl-chloro-dimethyl-silane (583 g, 3.88 mmoles) were added and stirred for three hours. The reaction was diluted with ethyl acetate (40 mL) and washed with water (50 mL) and brine (25 mL). The organic layer was dried with MgSO4 filtered and evaporated in vacuo. The crude product was purified by flash chromatography (hexanes:ethyl acetate 95:5 to 75:25) to give the title compound as a colorless oil.