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Acetonitrile → Methyl 3-ethoxy-4-(1-methylpyrazol-4-yl)benzoate

HRID 1096995
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1096995
[CH3:1][N:2]1[CH:6]=[CH:5][C:4](B2OC(C)(C)C(C)(C)O2)=[N:3]1.P([O-])([O-])([O-])=O.[K+].[K+].[K+].C(#N)C.Br[C:28]1[CH:37]=[CH:36][C:31]([C:32]([O:34][CH3:35])=[O:33])=[CH:30][C:29]=1[O:38][CH2:39][CH3:40]>O>[CH2:39]([O:38][C:29]1[CH:30]=[C:31]([CH:36]=[CH:37][C:28]=1[C:5]1[CH:4]=[N:3][N:2]([CH3:1])[CH:6]=1)[C:32]([O:34][CH3:35])=[O:33])[CH3:40]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 6342AcetonitrileHCID 62657Potassium Phosphate, TribasicHCID 27600771-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 66782630Methyl 4-bromo-3-ethoxybenzoate

Produkt 1

HCID 57930994Methyl 3-ethoxy-4-(1-methylpyrazol-4-yl)benzoate

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962
Water
Lösungsmittel

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

1-Methyl-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (183 mg, 0.88 mmol), potassium phosphate (374 mg, 1.76 mmol) and dichloro(1,1-bis(diphenylphosphino)-ferrocene)palladium(II) dichloromethane adduct (9.6 mg, 0.012 mmol) were added to an acetonitrile solution (3 mL) of methyl 4-bromo-3-ethoxybenzoate (152 mg, 0.59 mmol), and stirred overnight at 100° C. The reaction liquid was cooled to room temperature, and water was added to it. This was extracted with ethyl acetate, washed with saturated saline water, and dried with magnesium sulfate. The solution was filtered, and concentrated under reduced pressure, and the resulting residue was purified through silica gel column chromatography (hexane/ethyl acetate=50/50) to obtain the title compound as a white solid.

Aufarbeitung

  1. customThe reaction liquid
  2. temperaturewas cooled to room temperature
  3. extractionThis was extracted with ethyl acetate
  4. washwashed with saturated saline water
  5. dry with materialdried with magnesium sulfate
  6. filtrationThe solution was filtered
  7. concentrationconcentrated under reduced pressure
  8. customthe resulting residue was purified through silica gel column chromatography (hexane/ethyl acetate=50/50)

Quellen und Nachweise

ORD-Eintrag
ord-365589fdf9c54fb99f0feb703fbad90c
Quelldatensatz
uspto-grants-2012_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08138197B2

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