Reaktion #66059

Reaktionsgleichung

1-propanol

triethylamine

p-toluenesulfonyl chloride

HCl

→

propyl tosylate

Ausbeute 95.0%

Lösungsmittel

DCM

DCM

Reaktionsbedingungen

Aufarbeitung

1. 1
   TemperaturThe mixture was cooled to a temperature of about 5° C. to 15° C.
2. 2
   workup.ADDITIONOnce the addition
3. 3
   Temperaturthe mixture was warmed to a temperature of about 18° C. to 22° C.
4. 4
   Temperaturwhile maintaining the temperature below 25° C
5. 5
   SonstigeThe aqueous phase was removed
6. 6
   Waschenthe organic phase was washed 2× with water (21 L each wash)
7. 7
   Trocknendried with MgSO4
8. 8
   Filtrationfiltered over Celite®
9. 9
   WaschenThe filtered solids were then washed with DCM (4 L)
10. 10
    Einengenconcentrated to a residue
11. 11
    workup.DISSOLUTIONThe residue was dissolved in heptane
12. 12
    Einengenconcentrated again

Vorschrift

A 100 L glass, jacketed reactor was charged with 1-propanol (2.098 kg; 34.9 mol), triethylamine (4.585 kg; 45.3 mol; 1.3 equivalents) and DCM (20.1 L). The mixture was cooled to a temperature of about 5° C. to 15° C. and cautiously charged with a solution of p-toluenesulfonyl chloride (6 kg; 31.47 mol; 0.9 equivalents) in DCM (10.5 L) over 30 minutes. Once the addition was complete, the mixture was warmed to a temperature of about 18° C. to 22° C. and stirred for 12 hours. The reaction mixture was assayed by 1H NMR (in CDCl3) and deemed complete. HCl (6 N; 2.98 L) was cautiously charged while maintaining the temperature below 25° C. The aqueous phase was removed, and the organic phase was washed 2× with water (21 L each wash), dried with MgSO4, and filtered over Celite®. The filtered solids were then washed with DCM (4 L) and concentrated to a residue. The residue was dissolved in heptane and concentrated again to afford a final propyl tosylate product (6.385 kg, 95% yield).

Quelle