Reaktion #5500

Reaktionsgleichung

3-t-Butoxycarbonylmethyl-10-hydroxymethyl-2-oxo-1-azacyclodecane

Triethylamine

Thiolacetic acid

triethylamine

2-fluoro-1-methylpyridinium toluene-4-sulfonate

→

10-(acetylthiomethyl)-3-t-butoxycarbonylmethyl-2-oxo-1-azacyclodecane

Lösungsmittel

benzene

acetone

Reaktionsbedingungen

Aufarbeitung

1. 1
   Temperaturthe reaction is heated
2. 2
   Temperaturto reflux for 2 hours
3. 3
   SonstigeThe solvent is then removed
4. 4
   Sonstigethe crude product is partitioned between methylene chloride and water
5. 5
   Extraktionthe aqueous phase is extracted several times with methylene chloride
6. 6
   TrocknenThe combined organic layers are dried (MgSO4)
7. 7
   Sonstigethe solvent is evaporated
8. 8
   SonstigeThe crude product is purified by silica gel chromatography (15% ethyl acetate/hexane)

Vorschrift

3-t-Butoxycarbonylmethyl-10-hydroxymethyl-2-oxo-1-azacyclodecane (0.50 g, 1.67 mmol) is dissolved in acetone (5.0 mL) and benzene (5.0 mL). Triethylamine (0.26 mL, 1.9 mmol) is added, followed by 2-fluoro-1-methylpyridinium toluene-4-sulfonate (0.54 g, 1.9 mmol), and the reaction is stirred at room temperature for 90 minutes. Thiolacetic acid (0.14 mL, 1.9 mmol) and more triethylamine (0.26 mL, 1.9 mmol) are added, and the reaction is heated to reflux for 2 hours. The solvent is then removed, the crude product is partitioned between methylene chloride and water, and the aqueous phase is extracted several times with methylene chloride. The combined organic layers are dried (MgSO4) and the solvent is evaporated. The crude product is purified by silica gel chromatography (15% ethyl acetate/hexane) to give 10-(acetylthiomethyl)-3-t-butoxycarbonylmethyl-2-oxo-1-azacyclodecane, MS: M+1=358.

Quelle