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    ChemicalBook CAS DataBase List DIGLYCIDYL ETHER
    2238-07-5

    DIGLYCIDYL ETHER synthesis

    12synthesis methods
    -

    Yield:2238-07-5 67%

    Reaction Conditions:

    with Bu4NHSO4

    Steps:

    24.1 N-Methyl-N-[1-[2-hydroxy-3-[2-(4-methoxyphenyl)ethoxy]-propyl]-4-piperidyl]-4H-3,1-benzothiazin-2-amine Hydrogen Fumarate (24)
    24.1) 1-[2-(4-methoxyphenyl)ethoxy]-2,3-epoxypropane (24.1). By condensation of 4.8 g (31.5 mmol) of 4-methoxyphenethyl alcohol in a mixture of 25 ml of epichlorohydrin and 18 ml of 50% caustic soda and 430 mg of Bu4NHSO4 according to process 23.1, 4.42 g (yield: 67%) of glycidyl ether of formula 24.1 are prepared: Empirical formula: C12H16O3; Molecular mass: 208.25; Colorless oil; Boiling point: 130-135° C./0.25 mbar; NMR (CDCl3) δ: 2.6 (s, 1H); 2.78 (s, 1H); 2.79-2.91 (m, 2H); 3 (s, 1H); 3.34-3.5 (m, 1H); 3.5-3.89 (m, 3H); 3.9; (s, 3H); 6.83 (d, 2H); 7.14 (d, 2H).

    References:

    Pierre Fabre Medicament US6531469, 2003, B1

    FullText

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