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3-Chloro-4-fluorobenzaldehyde → (E)-ethyl 3-(3-chloro-4-fluorophenyl)-2-methylacrylate

HRID 514660
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HRID 514660 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][C:9]=1[F:10])[CH:5]=O.[C:11]([CH2:16][CH:17]=P(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)([O:13][CH2:14][CH3:15])=[O:12]>C1(C)C=CC=CC=1>[Cl:1][C:2]1[CH:3]=[C:4](/[CH:5]=[C:16](\[CH3:17])/[C:11]([O:13][CH2:14][CH3:15])=[O:12])[CH:7]=[CH:8][C:9]=1[F:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 5938663-Chloro-4-fluorobenzaldehydeHCID 12607919Ethyl 3-(triphenyl-lambda~5~-phosphanylidene)propanoate

생성물 1

HCID 86632358(E)-ethyl 3-(3-chloro-4-fluorophenyl)-2-methylacrylate수율 101.5%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

3-Chloro-4-fluorobenzaldehyde (10 g, 63.1 mmol) was dissolved in 300 mL toluene. (Carboethoxyethylidene)triphenylphosphorane (25 g, 69.4 mmol) was added and the mixture was heated to reflux overnight. The solution was cooled, diluted with hexanes and the solid was filtered. The filtrate was evaporated in vacuo, and the residue was dissolved in ether and filtered through a plug of silica using ether as eluent. The solvent was evaporated in vacuo to afford the title compound (15.55 g) as a semi solid. 1H NMR (300 MHz, CDCl3) δ ppm 7.56 (s, 1H), 7.44 (m, 1H), 7.23-7.32 (m, 1H), 7.16 (m, 1H), 4.28 (q, J=7.12 Hz, 2H), 2.09 (d, J=1.36 Hz, 3H), 1.35 (t, J=7.36 Hz, 3H). MS (DCI+) 243 (M+H).

후처리

  1. temperaturethe mixture was heated
  2. temperatureto reflux overnight
  3. temperatureThe solution was cooled
  4. filtrationthe solid was filtered
  5. customThe filtrate was evaporated in vacuo
  6. dissolutionthe residue was dissolved in ether
  7. filtrationfiltered through a plug of silica
  8. customThe solvent was evaporated in vacuo

출처 및 근거

ORD 기록
ord-8d65b0d21a464d6f9a655bd0675b29de
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09108905B2

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