Reaktion #571300

Reaktionsgleichung

NaHCO3

potassium hydride

6-bromo-4-(di-n-propylamino)-1,3,4,5-tetrahydrobenz[cd]indole

triisopropylsilyl triflate

→

(±)-6-Bromo-1-triisopropylsilyl-4-(di-n-propylamino)-1,3,4,5-tetrahydrobenz[cd]-indole

Lösungsmittel

THF

THF

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.STIRRINGStirring
2. 2
   workup.WAITwas continued for another hour
3. 3
   Extraktionthe product was extracted into CH2Cl2
4. 4
   WaschenThis extract was washed with NaCl solution
5. 5
   Trocknendried over Na2SO4
6. 6
   SonstigeEvaporation of the CH2Cl2
7. 7
   workup.WAITleft a brown oil which
8. 8
   Sonstigewas chromatographed over 50 g of silica gel
9. 9
   SonstigeThe silylated product from the column was isolated as a light brown oil in quantitative yield
10. 10
    SonstigeThe product slowly crystallized

Vorschrift

To a suspension of 1.25 g (7.50 mmol) of potassium hydride (24% dispersion in mineral oil) in 50 mL of THF at 0° C. was added a solution of 2.00 g (5.97 mmol) of 6-bromo-4-(di-n-propylamino)-1,3,4,5-tetrahydrobenz[cd]indole in 2 mL of THF. After stirring for 40 min, an addition of 1.90 mL (7.18 mmol) of triisopropylsilyl triflate was made. Stirring was continued for another hour. The mixture was then poured into cold NaHCO3 solution, and the product was extracted into CH2Cl2. This extract was washed with NaCl solution and dried over Na2SO4. Evaporation of the CH2Cl2 left a brown oil which was chromatographed over 50 g of silica gel using toluene followed by 1:3 EtOAc/toluene. The silylated product from the column was isolated as a light brown oil in quantitative yield. The product slowly crystallized upon standing.

Quelle