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Sodium Hydroxide → 1-(2,6-Dimethoxyphenyl)naphthalene

HRID 54027
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 54027
Br[C:2]1[C:7]([O:8][CH3:9])=[CH:6][CH:5]=[CH:4][C:3]=1[O:10][CH3:11].[C:12]1(OB(O)O)[C:21]2[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=2)[CH:15]=[CH:14][CH:13]=1.[OH-].[Na+]>O1CCOCC1.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>[C:20]1([C:2]2[C:7]([O:8][CH3:9])=[CH:6][CH:5]=[CH:4][C:3]=2[O:10][CH3:11])[C:21]2[C:16](=[CH:15][CH:14]=[CH:13][CH:12]=2)[CH:17]=[CH:18][CH:19]=1
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Komponenten

6

Edukt 3

HCID 14798Sodium HydroxideHCID 6122962-Bromo-1,3-dimethoxybenzeneHCID 13862914Naphthylboric acid

Produkt 1

HCID 154981511-(2,6-Dimethoxyphenyl)naphthaleneAusbeute 78,2 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 178418397HCID 178418397, VerbindungKatalysator
HCID 31275
1,4-Dioxane
Lösungsmittel

Versuchsvorschrift

To a solution of 1-bromo-2,6-dimethoxybenzene, (2.63 g, 12.1 mmol), tetrakis(triphenylphosphine)palladium (0) (0.91 g, 0.76 mol) and 1-naphthylboric acid (4.16 g, 23.9 mmol) in 1,4-dioxane (160 ml), a 2N aqueous solution of sodium hydroxide (13 ml) was added, and the mixture was heated to reflux. After cooling, the solvent was evaporated off, and the residue was dissolved in diethyl ether. The diethyl ether solution was washed with water and dried over anhydrous magnesium sulfate. Then, the solvent was evaporated off, and the residue was purified by silica gel column chromatography (developing phase: n-hexane/ethyl acetate=5/1) to obtain 1-naphthyl-2,6-dimethoxybenzene (2.50 g).

Aufarbeitung

  1. temperaturethe mixture was heated to reflux
  2. temperatureAfter cooling
  3. customthe solvent was evaporated off
  4. dissolutionthe residue was dissolved in diethyl ether
  5. washThe diethyl ether solution was washed with water
  6. dry with materialdried over anhydrous magnesium sulfate
  7. customThen, the solvent was evaporated off
  8. customthe residue was purified by silica gel column chromatography (developing phase: n-hexane/ethyl acetate=5/1)

Quellen und Nachweise

ORD-Eintrag
ord-0aae8bddb0dc42ebbc926bf057bf5887
Quelldatensatz
uspto-grants-1997_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05621129

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