Reaktion #82202
ord-24a572f086054e7eacbff4c2c637f301
Reaktionsgleichung
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1workup.ADDITIONAfter completion of addition
- 2workup.WAITto stand overnight
- 3Temperaturcooled in an ice bath
- 4SonstigeThe organic phase was separated
- 5Waschenthe aqueous layer was washed 3 times with diethyl ether
- 6TrocknenThe combined ethereal portions were dried over NaSO4
- 7Einengenconcentrated in vacuo
- 8Sonstigewas stored at -30° C.
- 9Sonstigeused 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.