반응 #1951066

ord-8fc686f44ee94aafa0c3cc30d7430a40

반응 방정식

O=P(Cl)(Cl)C1CC1
cyclopropyl phosphonic dichloride
C1CCOC1
THF
C=[CH][Mg][Br]
vinylmagnesium bromide
[Cl-].[NH4+]
NH4Cl
C=CP(=O)(C=C)C1CC1
cyclopropyl-divinyl-phosphine oxide
수율 39.0%

반응 조건

온도
-78°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타To a 250 mL round-bottom flask equipped with a magnetic stir-bar
  2. 2
    workup.ADDITIONpoured
  3. 3
    추출The resulting solution was extracted with DCM (3×100 mL)
  4. 4
    세척washed with brine (2×100 mL)
  5. 5
    건조dried over sodium sulfate
  6. 6
    농축concentrated in vacuo

실험 절차

To a 250 mL round-bottom flask equipped with a magnetic stir-bar was added cyclopropyl phosphonic dichloride (2.33 g, 14.7 mmol) and THF (100 mL). The solution was cooled to −78° C. and vinylmagnesium bromide (58.8 mmol, 1.0 M solution in THF) was added dropwise over 15 minutes. The solution was stirred at −78° C. for 7 hours and then poured, while still cold, into saturated aqueous NH4Cl (200 mL). The resulting solution was extracted with DCM (3×100 mL). The organic layers were combined, washed with brine (2×100 mL), dried over sodium sulfate and concentrated in vacuo to provide cyclopropyl-divinyl-phosphine oxide (0.811 g, 39%) as a light-brown free-flowing oil which was used without further purification. 1H NMR (400 MHz, CDCl3) δ 6.40-6.00 (m, 6H), 0.98-0.80 (m, 5H); GC-CIMS (m/z): (M+1)+ found, 142.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07625880B2uspto-grants-2009_12