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Dichloromethane → 4-[(1-Ethoxy)ethoxy]cinnamyl acetoacetate

HRID 2291356
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HRID 2291356 반응식
ClCCl.[CH2:4]([O:6][CH2:7][CH2:8][O:9][C:10]1[CH:19]=[CH:18][C:13]([CH:14]=[CH:15][CH2:16][OH:17])=[CH:12][CH:11]=1)[CH3:5].[CH2:20]=[C:21]1[O:25][C:23](=[O:24])[CH2:22]1>C([O-])(=O)C.[Na+].CCCCCC>[C:23]([O:17][CH2:16][CH:15]=[CH:14][C:13]1[CH:12]=[CH:11][C:10]([O:9][CH2:8][CH2:7][O:6][CH2:4][CH3:5])=[CH:19][CH:18]=1)(=[O:24])[CH2:22][C:21]([CH3:20])=[O:25]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 6344DichloromethaneHCID 12661Diketene2회HCID 545716914-[(1-Ethoxy)ethoxy]cinnamyl alcohol

생성물 1

HCID 542124814-[(1-Ethoxy)ethoxy]cinnamyl acetoacetate수율 90.7%

시약·촉매·용매 2

HCID 517045Sodium Acetate촉매HCID 8058Hexane
용매

실험 절차

36 Milliliters of dichloromethane was added to 12 g of 4-[(1-ethoxy)ethoxy]cinnamyl alcohol, then 60 mg of anhydrous sodium acetate was added thereto. Under refluxing condition, 5 g of diketene was added dropwise to the reaction mixture, and 2 hours later, 0.42 g diketene was further added thereto, the whole reaction mixture was refluxed for 1.5 hours. After the reaction was completed, the dichloromethane was removed by evaporation under reduced pressure, and the residue thus obtained was stirred for 30 minutes with 27 ml of hexane and 1.2 g of activated carbon. The activated carbon was removed by filtration, and the filtrate was concentrated to obtain 15 g of 4-[(1-ethoxy)ethoxy]cinnamyl acetoacetate as in the form of an oily substance.

후처리

  1. additionwas added dropwise to the reaction mixture, and 2 hours later
  2. customthe whole reaction mixture
  3. temperaturewas refluxed for 1.5 hours
  4. customthe dichloromethane was removed by evaporation under reduced pressure
  5. customthe residue thus obtained
  6. customThe activated carbon was removed by filtration
  7. concentrationthe filtrate was concentrated

출처 및 근거

ORD 기록
ord-2b0d5da75c5b4553bbf27d093634e087
출처 데이터셋
uspto-grants-1989_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04795814

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