반응 #1951062
ord-bb7c99bb198e4f6aa0bb3132d8627944
반응 방정식
반응 조건
후처리
- 1workup.STIRRINGstirred rapidly while the cold reaction mixture
- 2workup.ADDITIONwas added
- 3추출The product was extracted into dichloromethane
- 4세척washed with saturated aqueous sodium bicarbonate
- 5건조The organic phase was dried with sodium sulfate
- 6여과filtered
- 7농축concentrated by rotary evaporation
실험 절차
Cyclopropylmethyl-phosphonic dichloride (8.43 g, 48.7 mmol) was dissolved in dry THF (70 mL), placed under a nitrogen atmosphere, and chilled to −70° C. To this stirred solution was added dropwise vinyl magnesium bromide in THF (122 mL, 1 M). The resulting solution was stirred for 90 minutes at −70° C. An aqueous solution of ammonium chloride (500 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 3.56 g of (cyclopropylmethyl)-divinyl-phosphine oxide (22.8 mmol, 47%) as a white solid. 1H NMR (400 MHz, CDCl3) δ 6.44-6.14 (m, 6H); 1.84-1.78 (d of d, 2H) 0.98-0.86 (m, 1H); 0.66-0.60 (m, 2H); 0.25-0.19 (m, 2H); ESMS (m/z): (M+1)+ found, 157; (M−1)− found, 155.