PRODUCTION OF PROPYLENE CARBONATE
    23.
    发明专利

    公开(公告)号:JPH07267944A

    公开(公告)日:1995-10-17

    申请号:JP5892094

    申请日:1994-03-29

    摘要: PURPOSE:To provide an economically advantageous process for the production of propylene carbonate under milder reaction temperature and pressure condition at a high reaction rate in high yield by using an inexpensive alkali metal bromide and/or chloride as a catalyst. CONSTITUTION:This process for the production of propylene carbonate comprises the reaction of propylene oxide with carbon dioxide using an alkali metal bromide and/or chloride as a catalyst in the presence of 0.2-1 pt.wt. of an alcoholic solvent based on 1 pt.wt. of propylene oxide.

    PRODUCTION OF SPHINGOSINE USING TRIOL DERIVATIVE

    公开(公告)号:JPH0649054A

    公开(公告)日:1994-02-22

    申请号:JP16510093

    申请日:1993-06-10

    申请人: NOGUCHI KENKYUSHO

    摘要: PURPOSE:To efficiently obtain at a low cost in a stereoselective way sphingosine as the essential constituent of sphingoglycolipids by reaction of a phosphonic ester derivative with an aldehyde to form a diol derivative which is then reduced. CONSTITUTION:Firstly, a phosphonic ester derivative of formula I (R' is methyl, ethyl, phenyl or benzyl) is made to react with an aldehyde in the presence of a base (e.g. cesium carbonate) in a solvent (e.g. isopropyl alcohol) to form a (4E)-1,2-isopropylidene-3-oxo-4-alkene-1,2-diol derivative of formula II (R is

    29.
    发明专利
    失效

    公开(公告)号:JPH05247047A

    公开(公告)日:1993-09-24

    申请号:JP8138492

    申请日:1992-03-04

    申请人: SAGAMI CHEM RES

    摘要: PURPOSE:To obtain a new compound useful as an antitumor agent, having strong cell toxicity. CONSTITUTION:A compound of formula I (R is H or acyl; R is alkyl or aralkyl) such as (5R,7R,8S,11R,11aS)-7-cyano-5-hydroxymethyl-4-methoxy-13- methyl-5,7,8,9,10,11,11a,12-octahydro-8,11-azepino[1,2-b]isoquinoline. The compound of formula I is obtained by using 2-bromo-3-methylanisole of formula II as a starting substance, successively carrying out reactions to derive a compound of formula III (R is acyl; R is amino-protecting group), then replacing hydroxyl group at the 7-position of the compound of formula III with cyano group to give a compound of formula IV (R is H or amino-protecting group), eliminating the protecting group of amino group at the 13-position and alkylating or aralkylating the amino group at the 13-position.