Reaktion #1973459

ord-2f67d8811d954f05911e79e240b1f886

Reaktionsgleichung

CC(C)=O.O=S(=O)(O)O.[O]=[Cr](=[O])=[O]
Jones reagent
N#CC[C@H]1C[C@@H](CC=O)OC2(CCCCC2)O1
(±)-cis-4-(2-oxoethyl)-1,5-dioxaspiro[5.5]undecane-2-acetonitrile
CCOCC
diethyl ether
N#CC[C@@H]1C[C@H](CC(=O)O)OC2(CCCCC2)O1
(±)-cis-4-(cyanomethyl)-1,5-dioxaspiro[5.5]undecane-2-acetic acid

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Waschenwashed with brine until the aqueous washes
  2. 2
    TrocknenThe diethyl ether layer is dried (magnesium sulfate)
  3. 3
    Filtrationfiltered
  4. 4
    Einengenconcentrated

Vorschrift

Jones reagent (chromium trioxide-sulfuric acid-water), 4.4 mL (8.85 mmol), is added dropwise to a 0° C. solution of (±)-cis-4-(2-oxoethyl)-1,5-dioxaspiro[5.5]undecane-2-acetonitrile, 3.62 g (12.6 mmol), dissolved in 30 mL of acetone until the orange color is not discharged. After stirring a further 15 minutes, the mixture is poured into 300 mL of diethyl ether and washed with brine until the aqueous washes are colorless. The diethyl ether layer is dried (magnesium sulfate), filtered, and concentrated to provide 3.65 g of (±)-cis-4-(cyanomethyl)-1,5-dioxaspiro[5.5]undecane-2-acetic acid as a yellow solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05149837uspto-grants-1992_09