Reaktion #44624

ord-0de979c1ecc44607a3376da65e857d14

Lösungsmittel

Reaktionsbedingungen

Temperatur
0°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe resulting reaction solution
  2. 2
    workup.STIRRINGfurther stirred at 60° C. for 1 hr
  3. 3
    TemperaturThe reaction solution was cooled to room temperature
  4. 4
    workup.ADDITIONwas added
  5. 5
    SonstigeThe organic layer was separated
  6. 6
    Trocknendried over anhydrous magnesium sulfate
  7. 7
    Einengenconcentrated under reduced pressure
  8. 8
    SonstigeThe residue was purified by silica gel column chromatography (eluting solvent: heptane-ethyl acetate system)

Vorschrift

Bromoacetyl chloride (5.06 mL) was added to a solution mixture of toluene (100 mL) and a 2 N sodium hydroxide aqueous solution (100 mL) of (R)-(+)-2-amino-3-benzyloxy-1-propanol (10 g) under ice-cooling. The resulting reaction solution was stirred at 0° C. for 30 min and then further stirred at 60° C. for 1 hr. The reaction solution was cooled to room temperature, and a solution mixture of toluene and THF (1:1) was added thereto. The organic layer was separated, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluting solvent: heptane-ethyl acetate system) to give 1.36 g of the title compound. The physical property values of this compound were as follows:

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07737141B2uspto-grants-2010_06