Reaktion #1618040

ord-50e417f217424b1da3b46e06677be099

Reaktionsgleichung

CCCCCCCC/C=C\CCCCCCCC(=O)OCC(O)CO
2
CCCCCCCC/C=C\CCCCCCCC(=O)OCC(O)CO
cis-9-Octadecenoic acid 2,3-dihydroxypropyl ester
ClC(c1ccccc1)(c1ccccc1)c1ccccc1
triphenylmethyl chloride
CCCCCCCC/C=C\CCCCCCCC(=O)OCC(O)COC(c1ccccc1)(c1ccccc1)c1ccccc1
colorless oil
Ausbeute 88.0%
CCCCCCCC/C=C\CCCCCCCC(=O)OCC(O)COC(c1ccccc1)(c1ccccc1)c1ccccc1
cis-9-Octadecenoic acid 2-hydroxy-3-triphenylmethoxypropyl ester
Ausbeute 88.0%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe solvent is removed
  2. 2
    workup.ADDITIONthe residue is added twice with 50 ml of toluene
  3. 3
    Einengenconcentrated
  4. 4
    workup.ADDITIONThe residue is diluted with 100 ml of H2O
  5. 5
    Extraktionextracted three times with 50 ml of dichloromethane
  6. 6
    WaschenThe combined organic phases are washed with 50 ml of cold 5% HCl and 50 ml of saturated NaCl solution
  7. 7
    Trocknendried over MgSO4
  8. 8
    Filtrationfiltrated
  9. 9
    Einengenconcentrated
  10. 10
    SonstigeThe residue is purified by chromatography on silica gel

Vorschrift

A solution of 2 (21 mmol) in 80 ml of dichloromethane/pyridine (1:1) is added dropwise with triphenylmethyl chloride (27 mmol) and stirred at room temperature for 48 hours. The solvent is removed, and the residue is added twice with 50 ml of toluene and concentrated. The residue is diluted with 100 ml of H2O and extracted three times with 50 ml of dichloromethane. The combined organic phases are washed with 50 ml of cold 5% HCl and 50 ml of saturated NaCl solution, dried over MgSO4, filtrated and concentrated. The residue is purified by chromatography on silica gel using heptane/ethyl acetate (5:1). Yield: 88% of a colorless oil.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06197759B1uspto-grants-2001_03