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Acetic acid, 2-(triphenylphosphoranylidene)-, ethyl ester → HCID 59146165, 화합물

HRID 1512832
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HRID 1512832 반응식
[F:1][C:2]1[CH:3]=[C:4]2[C:8](=[C:9]([C:11]#[N:12])[CH:10]=1)[NH:7][CH:6]=[C:5]2[CH:13]=O.C1(P(=[CH:34][C:35]([O:37][CH2:38][CH3:39])=[O:36])(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>CC#N>[C:11]([C:9]1[CH:10]=[C:2]([F:1])[CH:3]=[C:4]2[C:8]=1[NH:7][CH:6]=[C:5]2/[CH:13]=[CH:34]/[C:35]([O:37][CH2:38][CH3:39])=[O:36])#[N:12]
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참가 물질

4

반응물 2

HCID 70670Acetic acid, 2-(triphenylphosphoranylidene)-, ethyl esterHCID 59146047HCID 59146047, 화합물

생성물 1

HCID 59146165HCID 59146165, 화합물수율 63.8%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

To a mixture of 5-fluoro-3-formyl-1H-indole-7-carbonitrile (D133) (8 g) in CH3CN (80 mL) was added ethyl (triphenylphosphoranylidene)acetate (30 g). The reaction was heated to reflux overnight. After the mixture was filtered, the filtrate was concentrated and purified by column chromatography to afford ethyl (2E)-3-(7-cyano-5-fluoro-1H-indol-3-yl)-2-propenoate (D134) (7 g) as a light yellow solid.

후처리

  1. temperatureThe reaction was heated
  2. temperatureto reflux overnight
  3. filtrationAfter the mixture was filtered
  4. concentrationthe filtrate was concentrated
  5. custompurified by column chromatography

출처 및 근거

ORD 기록
ord-b431221c7f2b4a4fbe09d07f30bff1ef
출처 데이터셋
uspto-grants-2012_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08217028B2

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