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Water → 2-Methyl-7-(4-dimethylaminophenyl)-1-indanone

HRID 1062931
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1062931
Br[C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:10]=1[C:9](=[O:11])[CH:8]([CH3:12])[CH2:7]2.[CH3:13][N:14]([CH3:24])[C:15]1[CH:20]=[CH:19][C:18](B(O)O)=[CH:17][CH:16]=1.C(=O)([O-])[O-].[Na+].[Na+].O>C(COC)OC.C([O-])(=O)C.[Pd+2].C([O-])(=O)C.C1(C)C=CC=CC=1C1C=CC=CC=1P(C1C=CC=CC=1C1C=CC=CC=1C)C1C=CC=CC=1C1C=CC=CC=1C>[CH3:12][CH:8]1[CH2:7][C:6]2[C:10](=[C:2]([C:18]3[CH:19]=[CH:20][C:15]([N:14]([CH3:24])[CH3:13])=[CH:16][CH:17]=3)[CH:3]=[CH:4][CH:5]=2)[C:9]1=[O:11]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 4

HCID 962WaterHCID 10340Sodium CarbonateHCID 27343444-(Dimethylamino)phenylboronic acidHCID 158697837-Bromo-2-methyl-2,3-dihydro-1H-inden-1-one

Produkt 1

HCID 158697842-Methyl-7-(4-dimethylaminophenyl)-1-indanoneAusbeute 76,5 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 167845
palladium(II) acetate
Katalysator
HCID 22172997Tris(o-tolylphenyl)phosphineKatalysator
HCID 80711,2-DimethoxyethaneLösungsmittel

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

Using a method similar to Example 22, 8.0 g (0.032 mol) of (2), 5.85 g (0.038 mol) of 4-dimethylaminophenylboronic acid and 7.4 g (0.07 mol) of sodium carbonate were placed in 122 ml of dimethoxyethane and 37 ml of water in the reaction vessel, the mixture was degassed a number of times and saturated with argon. 142 mg (0.6 mmol) of palladium acetate and 385 mg (1.3 mmol) of tris(o-tolylphenyl)phosphine were added and the reaction mixture was stirred for 4 hours at 80° C. After addition of 150 ml of water, the mixture was extracted 4 times with 100 ml each time of diethyl ether, the ether phase was washed twice with 50 ml each time of water and dried over magnesium sulfate. Removal of the solvent and column filtration through neutral aluminum oxide (dichloromethane) gave 6.5 g of 2-methyl-7-(4-dimethylaminophenyl)-1-indanone as an oil.

Aufarbeitung

  1. custom37 ml of water in the reaction vessel, the mixture was degassed a number of times
  2. extractionthe mixture was extracted 4 times with 100 ml each time of diethyl ether
  3. washthe ether phase was washed twice with 50 ml each time of water
  4. dry with materialdried over magnesium sulfate
  5. customRemoval of the solvent and column filtration through neutral aluminum oxide (dichloromethane)

Quellen und Nachweise

ORD-Eintrag
ord-ba2a083669044259ba4559b369679efc
Quelldatensatz
uspto-grants-2005_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06963017B2

Notizen zur Reaktion

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