3-Methoxybenzaldehyde → 3-methoxy-beta-methylstyrene Oxide

HRID 1074505

Reaktionsgleichung

Reaktionsgleichung von HRID 1074505
[C:1]1([SH+]C2C=CC=CC=2)C=CC=C[CH:2]=1.[CH3:14][O:15][C:16]1[CH:17]=[C:18]([CH:21]=[CH:22][CH:23]=1)[CH:19]=[O:20]>O1CCCC1>[CH3:14][O:15][C:16]1[CH:17]=[C:18]([CH:21]=[CH:22][CH:23]=1)[CH:19]1[O:20][CH:1]1[CH3:2]

Komponenten

4

Edukt 2

HCID 115693-MethoxybenzaldehydeHCID 22290449Diphenylsulfonium

Produkt 1

HCID 204969033-methoxy-beta-methylstyrene Oxide

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Reaktionsbedingungen

Temperatur
-78 °C

Versuchsvorschrift

To a -78° C. solution of diphenylsulfonium ethylide (1.0 mole) in tetrahydrofuran (one liter) is slowly added 3-methoxybenzaldehyde (1.0 mole). The reaction mixture is stirred at -78° C. for 3 hours and then allowed to warm to room temperature. It is then added to ether-water and the ether phase separated. The ether phase is washed with water, dried (MgSO4) and evaporated. Fractional distillation of the residue gives the title product.

Aufarbeitung

  1. customTo a -78° C.
  2. temperatureto warm to room temperature
  3. customthe ether phase separated
  4. washThe ether phase is washed with water
  5. dry with materialdried (MgSO4)
  6. customevaporated
  7. distillationFractional distillation of the residue

Quellen und Nachweise

ORD-Eintrag
ord-6972014de33f4bedb8bb86432fcf2cb7
Quelldatensatz
uspto-grants-1983_07
Patentnummer
US04391827

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