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Ethyl Acetate → HCID 19606368, Verbindung

HRID 1603915
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1603915
[CH:1]([C:3]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([C:12]([O:14][CH3:15])=[O:13])[CH:10]=2)[NH:5][CH:4]=1)=[O:2].CC(C)([O-])C.[K+].Br[CH2:23][CH2:24][CH2:25][CH2:26][C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1.C(OCC)(=O)C>CN(C)C=O>[C:27]1([CH2:26][CH2:25][CH2:24][CH2:23][N:5]2[C:6]3[C:11](=[CH:10][C:9]([C:12]([O:14][CH3:15])=[O:13])=[CH:8][CH:7]=3)[C:3]([CH:1]=[O:2])=[CH:4]2)[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 8857Ethyl AcetateHCID 2596681-Bromo-4-phenylbutaneHCID 19606277Methyl 3-formyl-1H-indole-5-carboxylateHCID 23665647Potassium tert-butoxide

Produkt 1

HCID 19606368HCID 19606368, VerbindungAusbeute 87 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228
Dimethylformamide
Lösungsmittel

Versuchsvorschrift

A solution of methyl 3-formylindole-5-carboxylate (2.234 g, 11.0 mmol) and potassium tert-butoxide (1.259 g, 11.2 mmol) in dry N,N-dimethylformamide (50 ml) was added with 1-bromo-4-phenylbutane (2.385 g, 11.2 mmol) and left under stirring at room temperature for 18 h. After that the solvent was evaporated off under reduced pressure, the resulting residue was partitioned between a NaCl saturated solution (50 ml) and chloroform (50 ml) and the aqueous phase was extracted with chloroform (3×50 ml). After drying and evaporating off the solvent under reduced pressure, a crude was obtained which was purified by chromatography through a silica gel column, eluting with n-hexane:ethyl acetate, 70:30, thereby obtaining 2.847 g of the title compound (87% yield).

Aufarbeitung

  1. waitleft
  2. customAfter that the solvent was evaporated off under reduced pressure
  3. customthe resulting residue was partitioned between a NaCl saturated solution (50 ml) and chloroform (50 ml)
  4. extractionthe aqueous phase was extracted with chloroform (3×50 ml)
  5. customAfter drying
  6. customevaporating off the solvent under reduced pressure
  7. customa crude was obtained which
  8. customwas purified by chromatography through a silica gel column
  9. washeluting with n-hexane

Quellen und Nachweise

ORD-Eintrag
ord-85a20250ed5f4d189e8e94bbf8c48387
Quelldatensatz
uspto-grants-1999_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05990142

Notizen zur Reaktion

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