Reaktion #1982187

Reaktionsgleichung

3-formyl-3-phenyl-pyrrolidine-1-carboxylic acid methyl ester

tert-Butyllithium

5-bromo-1-triisopropylsilanyl-1H-indole

→

3-[hydroxy-(1-triisopropylsilanyl-1H-indol-5-yl)-methyl]-3-phenyl-pyrrolidine-1-carboxylic acid methyl ester

Ausbeute 51.0%

Lösungsmittel

THF

THF

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.STIRRINGThe reaction mixture was stirred at −78° C. for 30 minutes
2. 2
   Temperaturwarmed to room temperature over a period of 1 hour
3. 3
   SonstigeThe reaction was quenched by addition of a saturated aqueous solution of NH4Cl
4. 4
   workup.ADDITIONdiluted with water
5. 5
   ExtraktionThe resulting mixture was extracted with EtOAc
6. 6
   Trocknenthe combined organic extracts were dried over MgSO4
7. 7
   Filtrationfiltered
8. 8
   Sonstigeevaporated under reduced pressure
9. 9
   SonstigeThe residue was purified by flash chromatography (10% to 50% of EtOAc in hexane)

Vorschrift

tert-Butyllithium (1.7 M in pentane, 8.9 mL, 15.10 mmol) was added at −78° C., under nitrogen atmosphere to a solution of 5-bromo-1-triisopropylsilanyl-1H-indole (2.42 g, 6.86 mmol) in THF (25 mL). The resulting pale yellow solution was stirred at −78° C. for 15 minutes, then a solution of 3-formyl-3-phenyl-pyrrolidine-1-carboxylic acid methyl ester (1.60 g, 6.86 mmol) in THF (5 mL) was then slowly added. The reaction mixture was stirred at −78° C. for 30 minutes and then warmed to room temperature over a period of 1 hour. The reaction was quenched by addition of a saturated aqueous solution of NH4Cl and diluted with water. The resulting mixture was extracted with EtOAc, and the combined organic extracts were dried over MgSO4, filtered and evaporated under reduced pressure. The residue was purified by flash chromatography (10% to 50% of EtOAc in hexane) to give 1.76 g (51% yield) of 3-[hydroxy-(1-triisopropylsilanyl-1H-indol-5-yl)-methyl]-3-phenyl-pyrrolidine-1-carboxylic acid methyl ester as a white foamy solid.

Quelle