Reaktion #549182
ord-408ee4819f684326b81cd60512a0e1a9
Reaktionsgleichung
Edukte
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1workup.STIRRINGstirred for ten minutes
- 2Sonstigerecooled to -30° C
- 3Temperaturto warm to 0° C
- 4workup.ADDITIONAdditional solvent is added
- 5workup.STIRRINGto facilitate stirring
- 6TemperaturThe mixture is maintained for 30 minutes at 0° C
- 7workup.ADDITIONpoured into 500 ml
- 8Extraktionof ethyl acetate, extracted with 100 ml
- 9Trocknenof aqueous saturated sodium chloride and dried over anhydrous magnesium sulfate
- 10Filtrationfiltered
- 11SonstigeThe filtrate is evaporated under vacuum
- 12Sonstigeaffording an oily residue which
- 13Sonstigeis then further purified by chromatography on silica gel eluting with 40% ethyl acetate-60% hexane, by vol.
Vorschrift
In this preparation 0.0525 mole of sodium hydride in a 50% mineral oil mixture is stirred in 300 ml. of anhydrous tetrahydrofuran, under nitrogen, then cooled to -30° C and 0.055 mole of glycidol is added dropwise. The mixture is allowed to warm to -5° C and stirred for ten minutes and then recooled to -30° C. A solution of 0.05 mole of 2-ethylsulfinyl-5-[2-(bicyclo[2.2.1]hept-7-yl)ethylaminocarbonyl]thiazole in 100 ml. of anhydrous tetrahydrofuran is added dropwise and the resulting mixture allowed to warm to 0° C. Additional solvent is added as needed to facilitate stirring. The mixture is maintained for 30 minutes at 0° C and then poured into 500 ml. of ethyl acetate, extracted with 100 ml. of water, and then with 100 ml. of aqueous saturated sodium chloride and dried over anhydrous magnesium sulfate and filtered. The filtrate is evaporated under vacuum affording an oily residue which is then further purified by chromatography on silica gel eluting with 40% ethyl acetate-60% hexane, by vol., affording 1,2-epoxy-3-(5-[2-(bicyclo[2.2.1]hept-7-yl)ethylaminocarbonyl]thiazole-2-yloxy)propane.