Triethyl phosphonoacetate → (E)-Ethyl 3-cyclobutylacrylate

HRID 1662497노트

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HRID 1662497 반응식
[Cl-].[Li+].C(OP([CH2:11][C:12]([O:14][CH2:15][CH3:16])=[O:13])(OCC)=O)C.[CH2:17]1[CH2:27][CH2:26]N2C(=NCCC2)[CH2:19][CH2:18]1.C1(C=O)CCC1>CC#N>[CH:18]1(/[CH:19]=[CH:11]/[C:12]([O:14][CH2:15][CH3:16])=[O:13])[CH2:17][CH2:27][CH2:26]1

참가 물질

6

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온도
0 °C

실험 절차

To a suspension of lithium chloride (2.22 g, 52.2 mmol) in MeCN (80 mL) were added ethyl 2-(diethoxyphosphoryl)acetate (available from Aldrich) (8.37 mL, 41.8 mmol) and DBU (16.7 mL, 111 mmol) at room temperature. The mixture was cooled to 0° C., and to it was added cyclobutanecarbaldehyde 70.B (2.93 g, 34.8 mmol) dropwise. The resulting cloudy mixture was warmed to room temperature and stirred overnight. The mixture was partitioned between water and EtOAc. The layers were separated, and the aqueous phase was extracted with additional EtOAc. The combined organic layers were washed with water and brine, dried (MgSO4), and concentrated. The residue was purified by silica gel flash chromatography (0-10% EtOAc/hexane) to afford (E)-ethyl 3-cyclobutylacrylate 70.C as a colorless liquid (5.00 g, 94%).

후처리

  1. temperatureThe resulting cloudy mixture was warmed to room temperature
  2. customThe mixture was partitioned between water and EtOAc
  3. customThe layers were separated
  4. extractionthe aqueous phase was extracted with additional EtOAc
  5. washThe combined organic layers were washed with water and brine
  6. dry with materialdried (MgSO4)
  7. concentrationconcentrated
  8. customThe residue was purified by silica gel flash chromatography (0-10% EtOAc/hexane)

출처 및 근거

ORD 기록
ord-6a7b0f6c26ab4ee99e6382156fa2025b
출처 데이터셋
uspto-grants-2011_10
특허 번호
US08030354B2

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