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Sodium Carbonate → 6-(4-Methoxyphenyl)naphthalene-2-carboxylic acid

HRID 858333
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 858333
Br[C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[CH:8]=[C:7]([C:12]([OH:14])=[O:13])[CH:6]=[CH:5]2.[CH3:15][O:16][C:17]1[CH:22]=[CH:21][C:20](B(O)O)=[CH:19][CH:18]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C([O-])([O-])=O.[Na+].[Na+]>C([O-])(=O)C.[Pd+2].C([O-])(=O)C.O.C(O)CC>[CH3:15][O:16][C:17]1[CH:22]=[CH:21][C:20]([C:2]2[CH:3]=[C:4]3[C:9](=[CH:10][CH:11]=2)[CH:8]=[C:7]([C:12]([OH:14])=[O:13])[CH:6]=[CH:5]3)=[CH:19][CH:18]=1
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Komponenten

8

Edukt 4

HCID 10340Sodium CarbonateHCID 11776TriphenylphosphineHCID 201262(4-Methoxyphenyl)boronic acidHCID 45498526-Bromo-2-naphthalenecarboxylic acid

Produkt 1

HCID 150998986-(4-Methoxyphenyl)naphthalene-2-carboxylic acidAusbeute 81 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 167845
palladium(II) acetate
Katalysator
HCID 962WaterLösungsmittel2×
HCID 10311-PropanolLösungsmittel

Versuchsvorschrift

In an 100 mL three-necked RB flask equipped with a magnetic bar, a condenser, and a nitrogen gas inlet, 6-bromo-2-naphthoic acid (2.62 g, 96%, 10 mmol), 4-methoxy-benzeneboronic acid (1.52 g, 10 mmol) and 1-propanol (20 mL) were mixed and stirred at room temperature for about 30 min. Palladium acetate (0.007 g, 0.003 equiv., 0.03 mmol), triphenylphosphine (0.024 g, 0.009 equiv., 0.9 mmol), Na2CO3 solution (2 M, 8 mL, 1.20 equiv., 12 mmol) and water (4 mL) were added and the mixture was refluxed for 2 h. When the mixture was still hot, 20 mL of water was added and the mixture was stirred and cooled to room temperature. The resultant crystals were filtered, washed with water and refluxed with 50 mL of acetic acid for 3–4 h. A white solid was obtained (2.55 g) and recrystallization from acetone gave the title compound as white crystals (2.24 g, 81%): mp 267–269° C.

Aufarbeitung

  1. customIn an 100 mL three-necked RB flask equipped with a magnetic bar, a condenser, and a nitrogen gas inlet
  2. temperaturethe mixture was refluxed for 2 h
  3. stirringthe mixture was stirred
  4. temperaturecooled to room temperature
  5. filtrationThe resultant crystals were filtered
  6. washwashed with water
  7. temperaturerefluxed with 50 mL of acetic acid for 3–4 h
  8. customA white solid was obtained
  9. custom(2.55 g) and recrystallization from acetone

Quellen und Nachweise

ORD-Eintrag
ord-9826da25b5fa4b07940a75b90b548d8e
Quelldatensatz
uspto-grants-2006_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07148311B2

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