Reaktion #6735

Reaktionsgleichung

sodium hydride

tetraethylene glycol

mesylate

tetraethylene glycol monobenzylether

→

title compound

Ausbeute 34.5%

Octaethylene Glycol Monobenzylether

Ausbeute 34.5%

Lösungsmittel

tetrahydrofuran

tetrahydrofuran

tetrahydrofuran

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.ADDITIONwas added dropwise
2. 2
   workup.STIRRINGthe reaction mixture was stirred overnight
3. 3
   SonstigeThe crude reaction mixture
4. 4
   Filtrationwas filtered through Celite (washed, CH2Cl2, 250 mL)
5. 5
   Waschenthe filtrate was washed H2O, dried MgSO4
6. 6
   Sonstigeevaporated to dryness
7. 7
   SonstigeThe resultant oil was chromatographed (silica, ethyl acetate/methanol, 10:1)
8. 8
   Sonstigechromatographed (silica, chloroform/methanol, 25:1)

Vorschrift

To a solution of tetrahydrofuran (140 mL) containing sodium hydride (0.43 g, 18 mmol) was added dropwise a solution of non-polydispersed tetraethylene glycol (3.5 g, 18 mmol) in tetrahydrofuran (10 mL) and the reaction mixture was stirred for 1 h. Then mesylate of non-polydispersed tetraethylene glycol monobenzylether 40 (6.0 g, 16.5 mmol) dissolved in tetrahydrofuran (10 mL) was added dropwise and the reaction mixture was stirred overnight. The crude reaction mixture was filtered through Celite (washed, CH2Cl2, 250 mL) and the filtrate was washed H2O, dried MgSO4, and evaporated to dryness. The resultant oil was chromatographed (silica, ethyl acetate/methanol, 10:1) and chromatographed (silica, chloroform/methanol, 25:1) to afford the non-polydispersed title compound as a clear oil (2.62 g, 34% yield).

Quelle