Process for preparing primary alkanols from 4,4-dialkyl-metadioxanes
    1.
    发明授权
    Process for preparing primary alkanols from 4,4-dialkyl-metadioxanes 失效
    从4,4-DIALKYL-METADIOXES制备主要烷基醇的方法

    公开(公告)号:US3541161A

    公开(公告)日:1970-11-17

    申请号:US72111968

    申请日:1968-04-12

    Applicant: MONTEDISON SPA

    CPC classification number: C07C29/103 C07C31/125

    Abstract: Monohydric alcohols, containing one carbon atom less than the parent metadioxane, are made by hydrogenolysis of 4,4-dialkyl metadioxanes, having a methyl or an ethyl group as one alkyl substituent and a C1 to C5 alkyl group as the other, with molecular hydrogen, in which a catalyst of Raney nickel, preferably 0.1 to 20% by weight, and zinc chloride, preferably 0.1 to 5% by weight of the metadioxane is used. A C1 to C4 alkanol is employed advantageously as solvent and preferred reaction conditions include 20 to 200 atmos. hydrogen pressure and 120 DEG to 220 DEG C. The starting material is made by condensation under mineral acid conditions of an olefine with aqueous formaldehyde. In the examples, 4 - methyl - 4 - propyl metadioxane, prepared from 2-methyl-1-pentene and aqueous formaldehyde, yields on hydrogenolysis, in methanol, 3-methyl hexanol.

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