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3-Fluoro-p-anisaldehyde → Ethyl 3-(3-fluoro-4-methoxyphenyl)-2-methylprop-2-enoate

HRID 62878
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인쇄 미리보기

반응식

HRID 62878 반응식
[F:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][C:9]=1[O:10][CH3:11])[CH:5]=O.[C:12]([CH2:17][CH:18]=P(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)([O:14][CH2:15][CH3:16])=[O:13]>C1COCC1>[CH2:15]([O:14][C:12](=[O:13])/[C:17](/[CH3:18])=[CH:5]/[C:4]1[CH:7]=[CH:8][C:9]([O:10][CH3:11])=[C:2]([F:1])[CH:3]=1)[CH3:16]
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참가 물질

4

반응물 2

HCID 676963-Fluoro-p-anisaldehydeHCID 12607919Ethyl 3-(triphenyl-lambda~5~-phosphanylidene)propanoate

생성물 1

HCID 75431686Ethyl 3-(3-fluoro-4-methoxyphenyl)-2-methylprop-2-enoate수율 99.5%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

반응 조건

온도
0 °C

실험 절차

After 3-fluoro-4-methoxy-benzaldehyde (0.50 g, 3.24 mmol) was dissolved in anhydrous THF (10 mL), carbethoxyethylidene triphenylphosphorane (1.75 g, 4.86 mmol) was added thereto at 0° C., and the mixture was stirred at room temperature for 3 hours. After the termination of the reaction, the reactant was concentrated under reduced pressure and purified by column chromatography (eluent, EtOAc/Hex=1/2) to obtain the title compound (0.768 g, 99%).

후처리

  1. customAfter the termination of the reaction
  2. concentrationthe reactant was concentrated under reduced pressure
  3. custompurified by column chromatography (eluent, EtOAc/Hex=1/2)

출처 및 근거

ORD 기록
ord-1d031625aaf242f59d8c7d4c9fd7f4b5
출처 데이터셋
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09447044B2

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