Reaktion #618601

Reaktionsgleichung

2-(2-(2-azidoethoxy)ethoxy)ethanol

triethylamine

tosyl chloride

→

2-(2-(2-azidoethoxy)ethoxy)ethyl 4-methylbenzenesulfonate

Ausbeute 90.0%

Lösungsmittel

—

Formula 8

methylene chloride

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeThe post-reaction mixture obtained
2. 2
   Sonstigewas partitioned
3. 3
   workup.DISTILLATIONto distilled water (40 mL) and ethyl acetate (120 mL)
4. 4
   SonstigeThe organic layer was separated
5. 5
   Waschenwashed with saturated salted water (15 mL)
6. 6
   Trocknendried with anhydrous sodium sulfate, and vacuum
7. 7
   workup.DISTILLATIONdistilled

Vorschrift

To a solution in which the 2-(2-(2-azidoethoxy)ethoxy)ethanol (3.05 g, 17.40 mmol) compound of Chemical Formula 8 was dissolved in methylene chloride (15 mL), 4-dimethylaminopyridine (DMAP) (212.6 mg, 1.74 mmol), triethylamine (TEA) (7.28 mL, 52.20 mmol) and tosyl chloride (3.98 g, 20.88 mmol) were added consecutively at room temperature. The post-reaction mixture obtained after stirring the reaction mixture for 12 hours at room temperature was partitioned to distilled water (40 mL) and ethyl acetate (120 mL). The organic layer was separated, washed with saturated salted water (15 mL), dried with anhydrous sodium sulfate, and vacuum distilled to give 2-(2-(2-azidoethoxy)ethoxy)ethyl 4-methylbenzenesulfonate (5.15 g, 90%). 1H NMR (500 MHz, CDCl3) δ 7.79 (d, 2H, J=8.2 Hz), 7.33 (d, 2H, J=8.2 Hz), 4.15 (t, 2H, J=5.0 Hz), 3.69 (t, 2H, J=5.0 Hz), 3.63 (t, 2H, J=5.5 Hz), 3.59 (s, 4H), 3.36 (t, 2H, J=5.0 Hz), 2.44 (s, 3H); 13C NMR (125 MHz, CDCl3) δ 144.9, 133.0, 129.9 (2), 128.0 (2), 70.8, 70.7, 70.1, 69.3, 68.8, 50.7, 21.7.

Quelle