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Ammonium Chloride → Ethyl 4-[3-(trifluoromethoxy)benzyl]benzoate

HRID 2359324
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2359324
[Cl-].[Li+].Br[CH2:4][C:5]1[CH:15]=[CH:14][C:8]([C:9]([O:11][CH2:12][CH3:13])=[O:10])=[CH:7][CH:6]=1.[F:16][C:17]([F:27])([F:26])[O:18][C:19]1[CH:20]=[C:21](Br)[CH:22]=[CH:23][CH:24]=1.CC(C1C=CC=C(C(C)C)C=1N1[C-]=[N+](C2C(C(C)C)=CC=CC=2C(C)C)CC1)C.[Cl-].[NH4+]>[Zn].CC(C1C=CC=C(C(C)C)C=1N1[CH-]N(C2C(C(C)C)=CC=CC=2C(C)C)CC1)C.C1C=NC=C(Cl)C=1.Cl[Pd]Cl.BrCCBr.C[Si](Cl)(C)C.C1COCC1>[F:16][C:17]([F:26])([F:27])[O:18][C:19]1[CH:24]=[C:23]([CH:22]=[CH:21][CH:20]=1)[CH2:4][C:5]1[CH:15]=[CH:14][C:8]([C:9]([O:11][CH2:12][CH3:13])=[O:10])=[CH:7][CH:6]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

11

Edukt 5

HCID 25517Ammonium ChlorideHCID 433294Lithium ChlorideHCID 5199641-Bromo-3-(trifluoromethoxy)benzeneHCID 954261Ethyl 4-(bromomethyl)benzoateHCID 10883669SIPr

Produkt 1

HCID 58046326Ethyl 4-[3-(trifluoromethoxy)benzyl]benzoate
Ausbeute 101,7 %

Reagenzien, Katalysatoren, Lösungsmittel 5

HCID 6397ChlorotrimethylsilaneKatalysatorHCID 78391,2-DibromoethaneKatalysatorHCID 23994ZincKatalysator2×HCID 588388791,3-Bis[2,6-di(propan-2-yl)phenyl]imidazolidin-2-ide;3-chloropyridine;dichloropalladiumKatalysatorHCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

A mixture of zinc (807 mg, 12.3 mmol) and lithium chloride (523 mg, 12.3 mmol) under argon was warmed for 10 minutes using a hot air gun, allowed to cool and then anhydrous THF (50 mL) added. The zinc was activated by treatment with 1,2-dibromoethane (39 mg, 0.21 mmol) and TMSCl (4.3 mg, 0.04 mmol). To the resulting mixture at 25° C. was added ethyl 4-(bromomethyl)benzoate (1.0 g, 4.15 mmol) and the mixture stirred for 15 minutes. 3-(Trifluoromethoxy)bromobenzene (694 mg, 2.88 mmol) was added, followed by (1,3-bis(2,6-diisopropylphenyl)imidazolidene)(3-chloropyridyl)palladium(II) dichloride [PEPPSI™-SIPr] (28 mg, 0.04 mmol) and the mixture stirred at 25° C. for 1 hour. Saturated ammonium chloride solution was added and the crude product extracted with ether. The ether extract was washed with brine, dried over Na2SO4 and the solvent evaporated in vacuo. The crude product was purified by silica gel column chromatography eluting with 7:3 hexane:ethyl acetate to afford the title compound (950 mg, 71%).

Aufarbeitung

  1. temperaturewas warmed for 10 minutes
  2. temperatureto cool
  3. stirringthe mixture stirred at 25° C. for 1 hour
  4. extractionthe crude product extracted with ether
  5. extractionThe ether extract
  6. washwas washed with brine
  7. dry with materialdried over Na2SO4
  8. customthe solvent evaporated in vacuo
  9. customThe crude product was purified by silica gel column chromatography
  10. washeluting with 7:3 hexane

Quellen und Nachweise

ORD-Eintrag
ord-42f1bf1861394012932bf6d5969b32ba
Quelldatensatz
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08685977B2

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