Reaktion #4466

ord-97da413a676c4eefa7c6d0c7176edaf1

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeA 500-ml, thick-walled Erlenynmeyer flask equipped with a magnetic stirring bar
  2. 2
    SonstigeThe cold bath was removed
  3. 3
    SonstigeThe reaction was quenched with 50 ml of saturated sodium bicarbonate
  4. 4
    Extraktionthe product extracted with ether
  5. 5
    TrocknenThe ether layer was dried over sodium sulfate
  6. 6
    Einengenconcentrated
  7. 7
    workup.DISTILLATIONAfter distillation

Vorschrift

A 500-ml, thick-walled Erlenynmeyer flask equipped with a magnetic stirring bar was cooled to -78° C. (dry iece-acetone bath) and charged with isobutylene (150 ml). Then, n-butyl glycolate (20.0 g, 0.151 mol) and 50 ml of methylene chloride was added along with 1 ml of concentrated sulfuric acid. The cold bath was removed and the mixture stirred for 3 days at room temperature. The reaction was quenched with 50 ml of saturated sodium bicarbonate and the product extracted with ether. The ether layer was dried over sodium sulfate and concentrated. After distillation, the title compound was obtained as a colorless oil: bp 64°-65° C. (0.7 mm).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04725620uspto-grants-1988_02