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Imidazole → 4-((Tert-butyldimethylsilyl)oxy)-2-fluorobenzonitrile

HRID 1873941
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1873941
[F:1][C:2]1[CH:9]=[C:8]([OH:10])[CH:7]=[CH:6][C:3]=1[C:4]#[N:5].N1C=CN=C1.[CH3:16][C:17]([Si:20](Cl)([CH3:22])[CH3:21])([CH3:19])[CH3:18]>CN(C=O)C>[Si:20]([O:10][C:8]1[CH:7]=[CH:6][C:3]([C:4]#[N:5])=[C:2]([F:1])[CH:9]=1)([C:17]([CH3:19])([CH3:18])[CH3:16])([CH3:22])[CH3:21]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 795ImidazoleHCID 28928tert-Butyldimethylsilyl chlorideHCID 27346752-Fluoro-4-hydroxybenzonitrile

Produkt 1

HCID 593707824-((Tert-butyldimethylsilyl)oxy)-2-fluorobenzonitrileAusbeute 73 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

2-Fluoro-4-hydroxybenzonitrile (30.1 g; manufactured by Wako Pure Chemical Industries, Ltd.) and imidazole (18.3 g; manufactured by Tokyo Chemical Industry Co., Ltd.) were dissolved in dehydrated DMF (436 mL; manufactured by Kanto Chemical Co., Inc.). After cooling to 0° C., TBDMSCl (48.3 g; manufactured by Tokyo Chemical Industry, Co., Ltd.) was added and the mixture was stirred for 1 hour while warming to room temperature. Solvent contained in the reaction solution was evaporated under reduced pressure. After adding water, extraction was carried out twice with ethyl acetate. The organic layer was washed twice with water and brine and dried over anhydrous sodium sulfate. After the solvent was evaporated under reduced pressure, purification was carried out with column chromatography (“COLUMN-A”; n-hexane:ethyl acetate=100:0→94:6) to obtain the title compound (40.3 g).

Aufarbeitung

  1. temperaturewhile warming to room temperature
  2. customwas evaporated under reduced pressure
  3. additionAfter adding
  4. extractionwater, extraction
  5. washThe organic layer was washed twice with water and brine
  6. dry with materialdried over anhydrous sodium sulfate
  7. customAfter the solvent was evaporated under reduced pressure, purification

Quellen und Nachweise

ORD-Eintrag
ord-e885c661ccc449c48c8ee1ca1fa19b62
Quelldatensatz
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08304443B2

Notizen zur Reaktion

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