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Ethyl cyanoacetate → Ethyl 2-chloro-2-cyano-5-oxopentanoate

HRID 2396573
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HRID 2396573 반응식
C([O-])([O-])=O.[K+].[K+].[C:7]([CH2:9][C:10](OCC)=[O:11])#N.Cl[C:16]([Cl:24])([C:22]#[N:23])[C:17]([O:19][CH2:20][CH3:21])=[O:18].C(C=C)=O>C(OCC)(=O)C>[Cl:24][C:16]([C:22]#[N:23])([CH2:7][CH2:9][CH:10]=[O:11])[C:17]([O:19][CH2:20][CH3:21])=[O:18]
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참가 물질

6

반응물 4

HCID 7764Ethyl cyanoacetateHCID 7847AcroleinHCID 11430Potassium CarbonateHCID 10997655Ethyl dichlorocyanoacetate

생성물 1

HCID 10998104Ethyl 2-chloro-2-cyano-5-oxopentanoate수율 77%

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매
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반응 조건

온도
5 °C

실험 절차

To a suspension of finely ground K2CO3 (4.26 g, 30 mmol) in 100 mL of ethyl acetate were added sequentially 5.65 g of ethyl cyanoacetate (50 mmol) and 9.1 g of ethyl dichlorocyanoacetate (50 mmol) at 0° C. Acrolein (6.72 g, 120 mmol) was added within a period of 1 h using a syringe pump. The resulting mixture was stirred at 5° C. for 3 hours, filtered through Celite with the aid of CH2Cl2, concentrated (25° C., 25 mm Hg), and distilled to give 15.6 of the title compound (77%).

후처리

  1. filtrationfiltered through Celite with the aid of CH2Cl2
  2. concentrationconcentrated (25° C., 25 mm Hg)
  3. distillationdistilled

출처 및 근거

ORD 기록
ord-56ef6a3692c0487d81c6bafbb62323e0
출처 데이터셋
uspto-grants-1996_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05493028

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