Reaktion #631990

ord-3ac98a95dbb941db8090677aa42dcb20

Reaktionsgleichung

Cl
HCl
CC(O)CC(=O)C1C(C)C=CCC1(C)C
3-hydroxy-1-(2,6,6-trimethyl-3-cyclohexen-1-yl)-1-butanone
c1ccncc1
pyridine
CCOC(=O)Cl
ethyl chloroformate
CCOC(=O)OC(C)CC(=O)C1C(C)C=CCC1(C)C
Ethyl 1-methyl-3-oxo-3-(2,6,6-trimethyl-3-cyclohexen-1-yl)propyl Carbonate

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionextracted twice with ether
  2. 2
    Waschenwashed (H2O, saturated aqueous NaHCO3
  3. 3
    Trocknenbrine), dried over Na2SO4
  4. 4
    Einengenconcentrated
  5. 5
    SonstigeThe oil (2.38 g) was purified by flash-chromatography (cyclohexane/AcOEt=98:2)

Vorschrift

A solution of 3-hydroxy-1-(2,6,6-trimethyl-3-cyclohexen-1-yl)-1-butanone (8.0 mmol) in pyridine (1.85 g, 23.4 mmol) was treated at 0° C. with ethyl chloroformate (1.24 g, 23.4 mmol). The reaction solution was stirred at room temperature for 36 hours, treated with 5% aqueous HCl and extracted twice with ether, washed (H2O, saturated aqueous NaHCO3, then brine), dried over Na2SO4 and concentrated. The oil (2.38 g) was purified by flash-chromatography (cyclohexane/AcOEt=98:2), using SiO2 (100 g). Yield: 2.06 g (78%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07935669B2uspto-grants-2011_05