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Diethyl Malonate → Diethyl 2-(3-butenyl)malonate

HRID 1458955
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HRID 1458955 반응식
CC[O-].[Na+].[Na].[C:6]([O:14][CH2:15][CH3:16])(=[O:13])[CH2:7][C:8]([O:10][CH2:11][CH3:12])=[O:9].Br[CH2:18][CH2:19][CH:20]=[CH2:21]>CCO>[CH2:21]([CH:7]([C:8]([O:10][CH2:11][CH3:12])=[O:9])[C:6]([O:14][CH2:15][CH3:16])=[O:13])[CH2:20][CH:19]=[CH2:18]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 7761Diethyl MalonateHCID 21241Homoallyl bromideHCID 2723922Sodium ethoxideHCID 5360545Sodium

생성물 1

HCID 594682Diethyl 2-(3-butenyl)malonate

시약·촉매·용매 1

HCID 702Ethanol용매2회

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온도
0 °C

실험 절차

A solution of NaOEt, prepared from the treatment of 1 L EtOH with sodium metal (19.5 g, 0.813 mol), was cooled to 0° C. and diethyl malonate (3-1, 100 g, 0.625 mol) was added dropwise over 0.5 h. After the addition was complete, the reaction was stirred for an additional 0.5 h, then a solution of 1-bromo-3-butene (76.1 mL, 0.75 mol) in 100 mL EtOH was added dropwise over forty-five minutes. The reaction was heated to reflux for 18 h, cooled and the solvent was removed in vacuo. The residue was dissolved in H2O and washed with EtOAc. The organic layer was dried with brine and MgSO4, filtered and evaporated. Fractional distillation of the residue (0.25-0.4 mm Hg, 70°-80° C.) gave 3-2 as a clear liquid.

후처리

  1. additionAfter the addition
  2. temperatureThe reaction was heated
  3. temperatureto reflux for 18 h
  4. temperaturecooled
  5. customthe solvent was removed in vacuo
  6. dissolutionThe residue was dissolved in H2O
  7. washwashed with EtOAc
  8. dry with materialThe organic layer was dried with brine and MgSO4
  9. filtrationfiltered
  10. customevaporated
  11. distillationFractional distillation of the residue (0.25-0.4 mm Hg, 70°-80° C.)

출처 및 근거

ORD 기록
ord-a600ad4f0efe48a592ff38be423e3ff1
출처 데이터셋
uspto-grants-1998_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05852045

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