Reaktion #82202

ord-24a572f086054e7eacbff4c2c637f301

Reaktionsbedingungen

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

Aufarbeitung

  1. 1
    workup.ADDITIONAfter completion of addition
  2. 2
    workup.WAITto stand overnight
  3. 3
    Temperaturcooled in an ice bath
  4. 4
    SonstigeThe organic phase was separated
  5. 5
    Waschenthe aqueous layer was washed 3 times with diethyl ether
  6. 6
    TrocknenThe combined ethereal portions were dried over NaSO4
  7. 7
    Einengenconcentrated in vacuo
  8. 8
    Sonstigewas stored at -30° C.
  9. 9
    Sonstigeused without further purification

Vorschrift

To a three neck 2 L round bottom flask charged with potassium t-butoxide (0.5 mol, 500 mL of a 1M solution in THF) and 500 mL of dry THF cooled to 0° C. was added dropwise from an addition funnel a solution of ethyl chloroacetate (0.5 mol, 53.5 mL) and ethyl formate (0.5 mol, 40.4 mL), in 200 mL of THF over 3 hours. After completion of addition, the reaction mixture was stirred for 1 hour and allowed to stand overnight. The resulting solid was diluted with diethyl ether and cooled in an ice bath. Then, the pH was lowered to approximately 3 using 6N HCl. The organic phase was separated, and the aqueous layer was washed 3 times with diethyl ether. The combined ethereal portions were dried over NaSO4, and concentrated in vacuo. The crude desired compound was stored at -30° C. and used without further purification.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05621109uspto-grants-1997_04