반응 #328149

ord-9adcd14b0c4a4fc99372caa67461f2dd

반응 조건

온도
50°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도was again cooled to 0° C.
  2. 2
    온도Next, the solution was warmed to 40° C.
  3. 3
    workup.STIRRINGstirred for 1 hour
  4. 4
    기타The reaction mixture was quenched with aq. HCl (10%, 88 ml)
  5. 5
    추출extracted with ether (3×45 ml)
  6. 6
    기타The organic fractions were collected
  7. 7
    건조dried over MgSO—4
  8. 8
    기타the solvent was removed in vacuo
  9. 9
    기타The crude oil was purified via silica gel chromatography (eluants: chloroform/hexane)

실험 절차

To a suspension of sodium hydride (5.0 g, 125 mmol) in HMPA (50 ml, distilled from calcium hydride) was added a solution of dimethyl malonate (11.7 ml, 100 mmol) in HMPA (5 ml) at 0° C. under argon. The mixture was heated to 50° C. and stirred 1 hour. Following this the solution was again cooled to 0° C., and a solution of 2,3-dibromopropene (12.2 ml, 100 mmol) in HMPA (5 ml) was added to the reaction mixture. Next, the solution was warmed to 40° C. and stirred for 1 hour. The reaction mixture was quenched with aq. HCl (10%, 88 ml) and extracted with ether (3×45 ml). The organic fractions were collected, dried over MgSO—4, and the solvent was removed in vacuo. The crude oil was purified via silica gel chromatography (eluants: chloroform/hexane) to obtain the titled product as a colorless oil (16.3 g, 65%). 1H-NMR (300 MHz, CDCl3) δ 5.70 (d, J=1.8 Hz, 1H), 5.48 (d, J=1.8 Hz, 1H), 3.63 (t, J=7.5 Hz, 1H), 3.76 (s, 6H), 3.04 (d, J=7.5 Hz, 2H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08648116B2uspto-grants-2014_02