反应 #1951058

ord-26f05ce324c149e2b0536f71ba21eb42

反应方程式

O=P(Cl)(Cl)Cc1ccc(F)cc1
4-Fluorobenzyl phosphonic dichloride
C1CCOC1
THF
C=[CH][Mg][Br]
vinyl magnesium bromide
C1CCOC1
THF
[Cl-].[NH4+]
ammonium chloride
C=CP(=O)(C=C)Cc1ccc(F)cc1
(4-fluorophenylmethyl) divinyl phosphine oxide
收率 84.0%

反应条件

温度
-70°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.STIRRINGstirred rapidly while the cold reaction mixture
  2. 2
    workup.ADDITIONwas added
  3. 3
    萃取The product was extracted into dichloromethane
  4. 4
    洗涤washed with saturated aqueous sodium bicarbonate
  5. 5
    干燥The organic phase was dried with sodium sulfate
  6. 6
    过滤filtered
  7. 7
    浓缩concentrated by rotary evaporation

实验过程

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.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07625880B2uspto-grants-2009_12