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Hexane → (3-Ethoxy-4-methoxy-phenyl)-(4-methoxy-3-methyl-phenyl)-methanol

HRID 2378276
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2378276
Br[C:2]1[CH:7]=[CH:6][C:5]([O:8][CH3:9])=[C:4]([O:10][CH2:11][CH3:12])[CH:3]=1.C([Li])CCC.CCCCCC.[CH3:24][O:25][C:26]1[CH:33]=[CH:32][C:29]([CH:30]=[O:31])=[CH:28][C:27]=1[CH3:34]>C1COCC1.O>[CH2:11]([O:10][C:4]1[CH:3]=[C:2]([CH:30]([C:29]2[CH:32]=[CH:33][C:26]([O:25][CH3:24])=[C:27]([CH3:34])[CH:28]=2)[OH:31])[CH:7]=[CH:6][C:5]=1[O:8][CH3:9])[CH3:12]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 8058HexaneHCID 1229363-Methyl-4-anisaldehydeHCID 217726904-Bromo-2-ethoxy-1-methoxybenzeneHCID 178418339Butyllithium

Produkt 1

HCID 69206060(3-Ethoxy-4-methoxy-phenyl)-(4-methoxy-3-methyl-phenyl)-methanol

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962
Water
Lösungsmittel
HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

To a solution of 4-bromo-2-ethoxy-1-methoxy-benzene (1.7 g, 7.4 mmol) in THF (20 mL) was added a solution of n-butyllitium in hexane (2.8 mL, 2.5 N, 7.0 mmol) at −78° C. and kept for 20 min. To the mixture was added 4-methoxy-3-methyl-benzaldehyde (1.0 g, 90% pure, 6.0 mmol) at −78° C. After 18 h, water (30 mL) was added to the mixture, and the cold bath was removed. The mixture was stirred at room temperature for 20 min. The mixture was extracted with ethyl acetate (2×50 mL). The combined organic layers was washed with HCl (0.5 N, 50 mL), sodium hydrogen carbonate (50 mL, sat), brine (50 mL) and dried over magnesium sulfate. Removal of solvent gave (3-ethoxy-4-methoxy-phenyl)-(4-methoxy-3-methyl-phenyl)-methanol as a solid (2.0 g, 100% crude yield). The sample was used in the next step without further purification.

Aufarbeitung

  1. waitAfter 18 h
  2. customthe cold bath was removed
  3. extractionThe mixture was extracted with ethyl acetate (2×50 mL)
  4. washThe combined organic layers was washed with HCl (0.5 N, 50 mL), sodium hydrogen carbonate (50 mL, sat), brine (50 mL)
  5. dry with materialdried over magnesium sulfate
  6. customRemoval of solvent

Quellen und Nachweise

ORD-Eintrag
ord-d3b74e1e0f7a4422b7c257bb8c3ef679
Quelldatensatz
uspto-grants-2008_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07470723B2

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