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4-Fluorobenzaldehyde → (E)-ethyl 3-(4-fluorophenyl)-2-methylacrylate

HRID 514655
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HRID 514655 반응식
[F:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=O)=[CH:4][CH:3]=1.[C:10]([CH2:15][CH:16]=P(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)([O:12][CH2:13][CH3:14])=[O:11]>C1(C)C=CC=CC=1>[F:1][C:2]1[CH:9]=[CH:8][C:5](/[CH:6]=[C:15](\[CH3:16])/[C:10]([O:12][CH2:13][CH3:14])=[O:11])=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 680234-FluorobenzaldehydeHCID 12607919Ethyl 3-(triphenyl-lambda~5~-phosphanylidene)propanoate

생성물 1

HCID 12016768(E)-ethyl 3-(4-fluorophenyl)-2-methylacrylate수율 99%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

4-Fluorobenzaldehyde (12 g, 97 mmol) was dissolved in toluene (500 mL). (Carboethoxyethylidene)triphenylphosphorane (42 g, 116 mmol) was added and the mixture was heated to reflux until the starting material was consumed. The solution was cooled, diluted with hexanes, and the solid was filtered. The filtrate was evaporated in vacuo. The remaining residue was dissolved in ether, and filtered through a plug of silica gel using ether as eluent. The solvents were evaporated in vacuo to afford the title compound (20 g, 99% yield) as a yellow solid. 1H NMR (DMSO-d6) δ ppm: 7.64 (s, 1H), 7.38 (dd, J=8.65, 5.59 Hz, 2H), 7.08 (t, J=8.65 Hz, 2H), 4.27 (q, J=7.12 Hz, 2H), 2.10 (d, J=1.36 Hz, 3H), 1.27-1.38 (m, 3H). MS (DCI+) 209 (M+H).

후처리

  1. temperaturethe mixture was heated
  2. temperatureto reflux until the starting material
  3. customwas consumed
  4. temperatureThe solution was cooled
  5. additiondiluted with hexanes
  6. filtrationthe solid was filtered
  7. customThe filtrate was evaporated in vacuo
  8. dissolutionThe remaining residue was dissolved in ether
  9. filtrationfiltered through a plug of silica gel
  10. customThe solvents were evaporated in vacuo

출처 및 근거

ORD 기록
ord-127f0236aefb4b079c8d76169d4c4d29
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09108905B2

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