Reaktion #549113

ord-0f8d4b5fbc2c4ff799fdbfd7f7f90394

Reaktionsbedingungen

Temperatur
-5°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.STIRRINGstirred for 10 minutes
  2. 2
    Sonstigerecooled to -30° C
  3. 3
    Temperaturto warm to 0° C
  4. 4
    workup.ADDITIONAdditional solvent is added
  5. 5
    workup.STIRRINGto facilitate stirring
  6. 6
    TemperaturThe mixture is maintained at 30 minutes at 0° C
  7. 7
    workup.ADDITIONpoured into 500 ml
  8. 8
    Extraktionof ethyl acetate, extracted with 100 ml
  9. 9
    Trocknenof aqueous saturated sodium chloride and dried over anhydrous magnesium sulfate
  10. 10
    Filtrationfiltered
  11. 11
    SonstigeThe filtrate is evaporated under vacuum
  12. 12
    Sonstigeaffording an oily residue which
  13. 13
    Sonstigeis 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 10 minutes and then recooled to -30° C. A solution of 0.05 mole of 2-ethylsulfonyl-5-(5-methylhex-3-ynylaminocarbonyl)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 at 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-(5-methylhex-3-ynylaminocarbonyl)thiazol-2-yloxy]propane.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04064257uspto-grants-1977_12