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Sodium hydride → 1-((2-(trimethylsilyl)ethoxy)methyl)-1H-indole-6-carbonitrile

HRID 2174092
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2174092
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[C:7]([C:10]#[N:11])[CH:8]=2)[CH:3]=[CH:2]1.[H-].[Na+].[CH3:14][Si:15]([CH2:18][CH2:19][O:20][CH2:21]Cl)([CH3:17])[CH3:16]>CN(C=O)C>[CH3:14][Si:15]([CH3:17])([CH3:16])[CH2:18][CH2:19][O:20][CH2:21][N:1]1[C:9]2[C:4](=[CH:5][CH:6]=[C:7]([C:10]#[N:11])[CH:8]=2)[CH:3]=[CH:2]1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 24758Sodium hydrideHCID 851461H-indole-6-carbonitrileHCID 27242712-Chloromethyl 2-(trimethylsilyl)ethyl ether

Produkt 1

HCID 867017281-((2-(trimethylsilyl)ethoxy)methyl)-1H-indole-6-carbonitrile

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

1H-Indole-6-carbonitrile (CAS #:15861-36-6) (1.47 g, 10.34 mmol) was dissolved in DMF (103 mL) and cooled to 0° C. NaH (60% in mineral oil, 0.620 g, 15.51 mmol) was added in one batch. The reaction was allowed to stir at room temperature for 15 minutes. SEMCl (2.38 mL, 13.44 mmol) was added at 0° C. and stirred for 20 minutes. The reaction was quenched with saturated ammonium chloride and then EtOAc was added. The organic layer was removed and the water layer was extracted again with EtOAc. The combined organics were washed with water, dried over MgSO4 filtered and concentrated. The resulting residue was purified via flash chromatography (0-50% EtOAc:heptanes) to obtain title compound. MS (ESI+) m/z 273.23 (M+H).

Aufarbeitung

  1. stirringstirred for 20 minutes
  2. customThe reaction was quenched with saturated ammonium chloride
  3. additionEtOAc was added
  4. customThe organic layer was removed
  5. extractionthe water layer was extracted again with EtOAc
  6. washThe combined organics were washed with water
  7. dry with materialdried over MgSO4
  8. filtrationfiltered
  9. concentrationconcentrated
  10. customThe resulting residue was purified via flash chromatography (0-50% EtOAc:heptanes)

Quellen und Nachweise

ORD-Eintrag
ord-294edd161127410d86008863fae613a8
Quelldatensatz
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09056874B2

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