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Water → {4-(Pentafluorophenyl)-2,3,5,6-tetrafluorophenyl}(triflyl)methane

HRID 1391860
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HRID 1391860 반응식
Br[CH2:2][C:3]1[C:8]([F:9])=[C:7]([F:10])[C:6]([C:11]2[C:16]([F:17])=[C:15]([F:18])[C:14]([F:19])=[C:13]([F:20])[C:12]=2[F:21])=[C:5]([F:22])[C:4]=1[F:23].[F:24][C:25]([F:30])([F:29])[S:26]([O-:28])=[O:27].[Na+].O.C(OCC)(=O)C>C(#N)CC>[F:17][C:16]1[C:11]([C:6]2[C:7]([F:10])=[C:8]([F:9])[C:3]([CH2:2][S:26]([C:25]([F:30])([F:29])[F:24])(=[O:28])=[O:27])=[C:4]([F:23])[C:5]=2[F:22])=[C:12]([F:21])[C:13]([F:20])=[C:14]([F:19])[C:15]=1[F:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 8857Ethyl AcetateHCID 23690734Sodium trifluoromethanesulfinateHCID 865911214-Bromomethylperfluorobiphenyl

생성물 1

HCID 22186455{4-(Pentafluorophenyl)-2,3,5,6-tetrafluorophenyl}(triflyl)methane수율 94%

시약·촉매·용매 1

HCID 7854
Propionitrile
용매

실험 절차

4-bromomethylperfluorobiphenyl (3.68 g, 9 mmol) and sodium trifluoromethane sulfinate (1.69 g, 10.8 mmol) were dissolved in propionitrile (30 mL), and the resultant solution was subjected to heating under reflux for 12 hours. After the reaction, the solution was cooled to room temperature, and water was added for extraction with ethyl acetate. The organic phase was dried with magnesium sulfate, filtrated, and the solvent was removed under reduced pressure. The crude product was purified by silica gel column chromatography (hexane-ethyl acetate=20:1 to 8:1 to 1:1), and the aimed {4-(pentafluorophenyl)-2,3,5,6-tetrafluorophenyl}(triflyl)methane (3.91 g, 8.46 mmol, 94% yield) was isolated. 1H NMR (CDCl3, 300 MHz) δ 4.75 (s, 2H, CH2Tf); 19F NMR (CDCl3, 282 MHz) δ−78.24 (s, 3F, CF3), −136.82 to −136.62 (m, 1F), −137.72 (dd, J=10.7, 18.3 Hz, 2F), −138.84 (dd, J=10.7, 18.3 Hz, 2F), −149.69 (t, J=21.3 Hz, 1F), −160.63 (dt, J=6.1, 21.3 Hz, 2F).

후처리

  1. temperatureto heating
  2. temperatureunder reflux for 12 hours
  3. customAfter the reaction
  4. dry with materialThe organic phase was dried with magnesium sulfate
  5. filtrationfiltrated
  6. customthe solvent was removed under reduced pressure
  7. customThe crude product was purified by silica gel column chromatography (hexane-ethyl acetate=20:1 to 8:1 to 1:1)

출처 및 근거

ORD 기록
ord-f39b7ab45c3b427a8aac35458b2c090d
출처 데이터셋
uspto-grants-2008_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07339082B2

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