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Water → Ethyl 3-(4-((4-chloro-3-ethylphenyl)oxy)phenyl)-3-oxo-2-((3-((1,1,2,2-tetrafluoroethyl)oxy)phenyl)methyl)propionate

HRID 1610488
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Reaktionsgleichung

Reaktionsgleichung von HRID 1610488
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][C:9]2[CH:14]=[CH:13][C:12]([C:15](=[O:22])[CH2:16][C:17]([O:19][CH2:20][CH3:21])=[O:18])=[CH:11][CH:10]=2)=[CH:4][C:3]=1[CH2:23][CH3:24].[H-].[Na+].[F:27][C:28]([F:41])([O:32][C:33]1[CH:34]=[C:35]([CH2:39]Br)[CH:36]=[CH:37][CH:38]=1)[CH:29]([F:31])[F:30].O>COCCOC>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][C:9]2[CH:10]=[CH:11][C:12]([C:15](=[O:22])[CH:16]([CH2:39][C:35]3[CH:36]=[CH:37][CH:38]=[C:33]([O:32][C:28]([F:27])([F:41])[CH:29]([F:30])[F:31])[CH:34]=3)[C:17]([O:19][CH2:20][CH3:21])=[O:18])=[CH:13][CH:14]=2)=[CH:4][C:3]=1[CH2:23][CH3:24]
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Komponenten

6

Edukt 4

HCID 962WaterHCID 24758Sodium hydrideHCID 114603781-(Bromomethyl)-3-(1,1,2,2-tetrafluoroethoxy)benzeneHCID 22262157Ethyl 3-(4-((4-chloro-3-ethylphenyl)oxy)phenyl)-3-oxopropionate

Produkt 1

HCID 22261529Ethyl 3-(4-((4-chloro-3-ethylphenyl)oxy)phenyl)-3-oxo-2-((3-((1,1,2,2-tetrafluoroethyl)oxy)phenyl)methyl)propionateAusbeute 58 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 80711,2-DimethoxyethaneLösungsmittel2×

Versuchsvorschrift

To a solution of 3-(1,1,2,2-tetrafluoroethoxy)toluene (6.0 g, 28.8 mmol) in carbon tetrachloride (60 ml) were added N-bromosuccinimide (5.65 g, 31.7 mmol) and 2,2′-azobis(isobutyronitrile) (237 mg, 1.44 mmol), and the mixture was heated under reflux for 6 hrs. After cooling, the reaction solution was filtered, and the filtrate was concentrated to give 3-(1,1,2,2-tetrafluoroethoxy)-α-bromotoluene. To a solution of ethyl 3-(4-((4-chloro-3-ethylphenyl)oxy)phenyl)-3-oxopropionate (10 g, 28.8 mmol) in 1,2-dimethoxyethane (100 ml) was added sodium hydride (60% in oil, 1.15 g, 28.8 mmol) under ice-cooling, and the mixture was stirred at room temperature for 30 min. To the reaction solution was dropwise added a solution of 3-(1,1,2,2-tetrafluoroethoxy)-α-bromotoluene prepared earlier in 1,2-dimethoxyethane (10 ml), and the reaction solution was stirred at room temperature for 1 hr. The reaction solution was poured into water (100 ml), and the mixture was extracted with ethyl acetate (100 ml×2). The extract was washed with water and saturated brine, dried over anhydrous magnesium sulfate and evaporated under reduced pressure. The residue was purified by silica gel column chromatography (toluene) to give ethyl 3-(4-((4-chloro-3-ethylphenyl)oxy)phenyl)-3-oxo-2-((3-((1,1,2,2-tetrafluoroethyl)oxy)phenyl)methyl)propionate (9.26 g, 58%) as a colorless oil.

Aufarbeitung

  1. temperaturecooling
  2. stirringthe reaction solution was stirred at room temperature for 1 hr
  3. extractionthe mixture was extracted with ethyl acetate (100 ml×2)
  4. washThe extract was washed with water and saturated brine
  5. dry with materialdried over anhydrous magnesium sulfate
  6. customevaporated under reduced pressure
  7. customThe residue was purified by silica gel column chromatography (toluene)

Quellen und Nachweise

ORD-Eintrag
ord-20080dcba3274a8bb0be8b5cf0ad1b49
Quelldatensatz
uspto-grants-2006_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06982348B2

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