StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
  1. Startseite
  2. /Reaktion

Toluene → Methyl 2-methoxy-2'-methylbiphenyl-4-carboxylate

HRID 639234
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 639234
[C:1]1([CH3:7])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.Br[C:9]1[CH:18]=[CH:17][C:12]([C:13]([O:15][CH3:16])=[O:14])=[CH:11][C:10]=1[O:19][CH3:20].C1(C)C=CC=CC=1B(O)O.C(=O)([O-])[O-].[Na+].[Na+]>C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.O.C(O)C>[CH3:16][O:15][C:13]([C:12]1[CH:17]=[CH:18][C:9]([C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][C:1]=2[CH3:7])=[C:10]([O:19][CH3:20])[CH:11]=1)=[O:14]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 4

HCID 1140TolueneHCID 10340Sodium CarbonateHCID 27332672-Methylphenyl boronic acidHCID 14570117Methyl 4-bromo-3-methoxybenzoate

Produkt 1

HCID 53941402Methyl 2-methoxy-2'-methylbiphenyl-4-carboxylateAusbeute 99 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 178418397
HCID 178418397, Verbindung
Katalysator
HCID 702EthanolLösungsmittel
HCID 962WaterLösungsmittel

Reaktionsbedingungen

Temperatur
105 °C

Versuchsvorschrift

A solution consisting of toluene (100 mL), ethanol (50 mL), and water (50 mL) was sparged with dry nitrogen for 45 minutes. To the mixture was added methyl 4-bromo-3-methoxybenzoate of step B (26.5 mmol), o-tolylboronic acid (29.1 mmol), and sodium carbonate (112.5 mmol). The mixture was sparged with nitrogen for an additional ten minutes. Terakis(triphenylphosphine)palladium(0) (1 mmol) was added to the mixture, which was then heated at 105° C. for 6 hours. The mixture was cooled and the organic phase was washed three times in sequence with saturated aqueous sodium carbonate and brine. The organics were dried over anhydrous sodium sulfate, filtered, and evaporated to an oil. Flash chromatography of the residue on silica gel using dichloromethane/hexane (3:1) yielded the title compound as a clear oil (6.7 g, 99%).

Aufarbeitung

  1. customwas sparged with dry nitrogen for 45 minutes
  2. customThe mixture was sparged with nitrogen for an additional ten minutes
  3. temperatureThe mixture was cooled
  4. washthe organic phase was washed three times in sequence with saturated aqueous sodium carbonate and brine
  5. dry with materialThe organics were dried over anhydrous sodium sulfate
  6. filtrationfiltered
  7. customevaporated to an oil

Quellen und Nachweise

ORD-Eintrag
ord-74b5282b58404899945b3ccd7801d262
Quelldatensatz
uspto-grants-2010_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07691848B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion