Methyl iodide → 3,4-Dimethoxyphenyl-1-methoxybutane

HRID 1031794Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1031794
[H-].[Na+].[CH3:3][O:4][C:5]1[CH:6]=[C:7]([CH:13]([OH:27])[CH2:14][CH2:15][CH2:16]C2C=CC(OC)=C(OC)C=2)[CH:8]=[CH:9][C:10]=1[O:11][CH3:12].CI.[CH2:30]1COCC1>O>[CH3:3][O:4][C:5]1[CH:6]=[C:7]([CH:13]([O:27][CH3:30])[CH2:14][CH2:15][CH3:16])[CH:8]=[CH:9][C:10]=1[O:11][CH3:12]

Komponenten

6

Edukt 4

HCID 6328Methyl iodide2×HCID 8028TetrahydrofuranHCID 24758Sodium hydrideHCID 148526081,4-Bis(3,4-dimethoxyphenyl)butane-1-ol

Produkt 1

HCID 221684663,4-Dimethoxyphenyl-1-methoxybutane

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

A 60% dispersion of NaH in mineral oil (32.7 g, 1.3625 mole) was added portionwise over 40 minutes to a mechanically stirred solution of 1,4-bis (3,4-dimethoxyphenyl)butane-1-ol (292 g, 0.843 mole), MeI (125.4 g, 0.883 mole, 55 cc), and dry THF (1.5 1) at 22°-33° C. maintained by intermittent cooling. Additional MeI (22.8 g, 0.16 mole, 10 cc) was added and the reaction mixture was stirred overnight at room temperature. The reaction mixture was treated with H2O (15 cc), stirred for 1 hour, and filtered. The filtrate was evaporated in vacuo to a syrup; the syrup was treated with CH2Cl2 (1 1) and H2O (500 cc) and the phases were separated. The aqueous phase was extracted with CH2Cl2 (1×500 cc). The combined organic phase was washed with H2O (3×400 cc), dried (Na ) and evaporated in vacuo to a yellow syrup; yield: 293 g (96%).

Aufarbeitung

  1. temperaturemaintained by intermittent cooling
  2. stirringstirred for 1 hour
  3. filtrationfiltered
  4. customThe filtrate was evaporated in vacuo to a syrup
  5. additionthe syrup was treated with CH2Cl2 (1 1) and H2O (500 cc)
  6. customthe phases were separated
  7. extractionThe aqueous phase was extracted with CH2Cl2 (1×500 cc)
  8. washThe combined organic phase was washed with H2O (3×400 cc)
  9. customdried (Na )
  10. customevaporated in vacuo to a yellow syrup

Quellen und Nachweise

ORD-Eintrag
ord-8fa8422822dd490098e6147edff13127
Quelldatensatz
uspto-grants-1990_09
Patentnummer
US04954659

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