Reaktion #1951058

Reaktionsgleichung

4-Fluorobenzyl phosphonic dichloride

THF

vinyl magnesium bromide

THF

ammonium chloride

→

(4-fluorophenylmethyl) divinyl phosphine oxide

Ausbeute 84.0%

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.STIRRINGstirred rapidly while the cold reaction mixture
2. 2
   workup.ADDITIONwas added
3. 3
   ExtraktionThe product was extracted into dichloromethane
4. 4
   Waschenwashed with saturated aqueous sodium bicarbonate
5. 5
   TrocknenThe organic phase was dried with sodium sulfate
6. 6
   Filtrationfiltered
7. 7
   Einengenconcentrated by rotary evaporation

Vorschrift

4-Fluorobenzyl phosphonic dichloride (1.71 g, 7.82 mmol) was dissolved in 10 mL of dry THF, under a nitrogen atmosphere, and chilled to −70° C. To this stirred solution was added dropwise vinyl magnesium bromide in THF (18.3 mL, IM). The resulting solution was stirred for 30 minutes at −70° C. An aqueous solution of ammonium chloride (100 mL, 2 M) was chilled to 0° C. and stirred rapidly while the cold reaction mixture was added. The product was extracted into dichloromethane and washed with saturated aqueous sodium bicarbonate, and then with water. The organic phase was dried with sodium sulfate, filtered, and concentrated by rotary evaporation to yield 1.375 g of (4-fluorophenylmethyl) divinyl phosphine oxide (6.55 mmol, 84%) as a white solid. 1H NMR (400 MHz, CDCl3) 7.20-7.14 (m, 2H); 7.01-6.95 (m 2H); 6.29-6.08 (m, 6H); 3.20-3.15 (d, 2H); ESMS (m/z): (M+1)+found, 211.

Quelle