Water → 4-(4-Methoxyphenyl)-1-(3-methylbutyl)-1H-pyrazole

HRID 250512

Reaktionsgleichung

Reaktionsgleichung von HRID 250512
Br[C:2]1[CH:7]=[CH:6][C:5]([O:8][CH3:9])=[CH:4][CH:3]=1.[CH3:10][CH:11]([CH3:28])[CH2:12][CH2:13][N:14]1[CH:18]=[C:17](B2OC(C)(C)C(C)(C)O2)[CH:16]=[N:15]1.C(=O)([O-])[O-].[K+].[K+].O>O1CCCC1.C1C=CC(P([C]2[CH][CH][CH][CH]2)C2C=CC=CC=2)=CC=1.C1C=CC(P([C]2[CH][CH][CH][CH]2)C2C=CC=CC=2)=CC=1.Cl[Pd]Cl.[Fe]>[CH3:9][O:8][C:5]1[CH:6]=[CH:7][C:2]([C:17]2[CH:16]=[N:15][N:14]([CH2:13][CH2:12][CH:11]([CH3:28])[CH3:10])[CH:18]=2)=[CH:3][CH:4]=1

Komponenten

7

Edukt 4

HCID 962WaterHCID 77304-BromoanisoleHCID 11430Potassium CarbonateHCID 27598311-(3-Methylbutyl)-1H-pyrazole-4-boronic acid pinacol ester

Produkt 1

HCID 112880284-(4-Methoxyphenyl)-1-(3-methylbutyl)-1H-pyrazoleAusbeute 127,4 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 178477754HCID 178477754, VerbindungKatalysatorHCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

To p-bromoanisole (0.25 g, 1.33 mmol) was added a solution of 1-(3-methylbutyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (0.41 g, 1.55 mmol) in tetrahydrofuran (10 ml), potassium carbonate (0.29 g, 2.1 mmol) and [1,1-bis(diphenylphosphino)ferrocene]dichloropalladium (II) (12 mg, 0.023 mmol) and the mixture refluxed under nitrogen for 17 h. Water (50 ml) was added to the reaction mixture and stirring continued at RT for 15 min followed by extraction with ether (2×50 ml), drying (MgSO4) and evaporation of the ether extract to give a brown oil (0.414 g). Purification by column chromatography (silica gel, 100% chloroform) afforded 4-(4-methoxyphenyl)-1-(3-methylbutyl)-1H-pyrazole (12) as a waxy pale yellow solid (37 mg, 11%). 1H nmr (CDCl3, 300 MHz) 0.97, d (6.6 Hz), 2×Me; 1.64, sept (6.6 Hz), H3″; 1.80, dt (7.2 Hz), H2″; 3.82, s, OMe; 4.15, t (7.5 Hz), H1″; 6.90, d (8.7 Hz), H3′,5′; 7.39, d (8.7 Hz), H2′,6′; 7.54, s, H3 or H5; 7.69, s, H5 or H3. ESI (+ve) MS m/z 245 (M+H, 100%).

Aufarbeitung

  1. temperaturethe mixture refluxed under nitrogen for 17 h
  2. extractionfollowed by extraction with ether (2×50 ml)
  3. customdrying
  4. custom(MgSO4) and evaporation of the ether
  5. extractionextract

Quellen und Nachweise

ORD-Eintrag
ord-f08da7ac3fa24a7584799519aa8d4db6
Quelldatensatz
uspto-grants-2011_01
Patentnummer
US07863313B2

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