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Ethyl cyanoacetate → 2-Propenoic acid, 2-cyano-3-(4-cyanophenyl)-, ethyl ester

HRID 1766349
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HRID 1766349 반응식
[C:1]([C:3]1[CH:10]=[CH:9][C:6]([CH:7]=O)=[CH:5][CH:4]=1)#[N:2].[C:11]([CH2:13][C:14]([O:16][CH2:17][CH3:18])=[O:15])#[N:12].N1CCCCC1>C(O)C>[CH2:17]([O:16][C:14](=[O:15])[C:13]([C:11]#[N:12])=[CH:7][C:6]1[CH:9]=[CH:10][C:3]([C:1]#[N:2])=[CH:4][CH:5]=1)[CH3:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7764Ethyl cyanoacetateHCID 8082PiperidineHCID 660424-Cyanobenzaldehyde

생성물 1

HCID 3670612-Propenoic acid, 2-cyano-3-(4-cyanophenyl)-, ethyl ester

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

4-Cyanobenzaldehyde (3.00 g, 22.9 mmol) ad ethyl cyanoacetate (2.59 g, 22.9 mmol) are dissolved in absolute ethanol (100 ml). Piperidine (0.097 g, 1.14 mmol) is added, and the solution is stirred at room temperature until no more starting material is apparent by tic. This takes approx. 2 hours during which time a precipitate is formed. The precipitate is filtered and recrystallised, or alternatively, the crude reaction mixture is concentrated in vacuo and chromatographed over silica with cyclohexane/ethyl acetate mixtures as eluent to yield a white solid.

후처리

  1. customThis takes approx. 2 hours during which time a precipitate is formed
  2. filtrationThe precipitate is filtered
  3. customrecrystallised
  4. customalternatively, the crude reaction mixture
  5. concentrationis concentrated in vacuo
  6. customchromatographed over silica with cyclohexane/ethyl acetate
  7. customto yield a white solid

출처 및 근거

ORD 기록
ord-6481639f81844518b0a047ed27ccd219
출처 데이터셋
uspto-grants-2007_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07230017B2

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