Reaktion #159785

Reaktionsgleichung

(2-bromo-5-iodo-phenyl)-chroman-6-yl-methanone

triethylsilane

→

6-(2-bromo-5-iodo-benzyl)-chroman

Ausbeute 77.5%

Lösungsmittel

acetonitrile dichloromethane

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigereaction
2. 2
   Sonstigewas quenched by the addition of saturated aqueous sodium bicarbonate solution
3. 3
   SonstigeVolatiles were evaporated under reduced pressure
4. 4
   ExtraktionThe aqueous layer was extracted with ethyl acetate (2×20 mL)
5. 5
   WaschenEthyl acetate layer was washed with water, brine
6. 6
   Trocknendried over sodium sulfate
7. 7
   Einengenconcentrated
8. 8
   Sonstigepurified by silica gel column chromatography

Vorschrift

To a stirred solution of (2-bromo-5-iodo-phenyl)-chroman-6-yl-methanone (2.0 g, 4.51 mmol) in acetonitrile: dichloromethane (2:1 mixture, 9 mL) was added triethylsilane (2.52 mL, 15.78 mmol) and boron trifluoride diethyl etherate complex 1.11 mL, 9.02 mmol) at 0° C. After stirring overnight at room temperature, reaction was quenched by the addition of saturated aqueous sodium bicarbonate solution. Volatiles were evaporated under reduced pressure. The aqueous layer was extracted with ethyl acetate (2×20 mL). Ethyl acetate layer was washed with water, brine, dried over sodium sulfate, concentrated and purified by silica gel column chromatography to furnish 6-(2-bromo-5-iodo-benzyl)-chroman (1.5 g).

Quelle