发明名称 PRODUCTION OF CINNAMIC ACID DERIVATIVE
摘要 PURPOSE:To readily obtain a cinnamic acid derivative in high yield and purity in a short time without coloring of a reaction solution, etc., by reacting a benzaldehyde derivative with a malonic acid derivative in the presence of a specific aminopyridine derivative as a catalyst. CONSTITUTION:A benzaldehyde derivative expressed by formula I {R<1> and R<2> are H, OH, nitro, lower alkyl, lower alkoxy, -NR<3>R<4> [R<3> and R<4> are H, (halogen-substituted) lower alkyl, etc.}, etc. is reacted with a malonic acid derivative expressed by formula II (R<5> is H or lower alkyl) in an inert solvent in the presence of an aminopyridine derivative catalyst expressed by formula III (R<6> and R<7> are R<5> or together with N form a 5- or 6-membered saturated heterocyclic ring), e.g. 4-dimethylaminopyridine, etc., at 0-200 deg.C for 1-15hr to afford the aimed compound expressed by formula IV. EFFECT:The reaction solvent and catalyst are readily recovered and regenerated and working environment is good. Industrial massproduction can be carried out without requiring deodorizing equipment. USE:An intermediate for synthesizing medicines.
申请公布号 JPS62281840(A) 申请公布日期 1987.12.07
申请号 JP19860124980 申请日期 1986.05.29
申请人 OTSUKA PHARMACEUT CO LTD 发明人 NISHIDA YOSHIYUKI;KAWASAKI KENGO;TAKADA SHIGERU
分类号 C07B61/00;B01J31/00;B01J31/02;C07C51/00;C07C51/353;C07C57/42;C07C57/44;C07C59/52;C07C59/64;C07C67/00;C07C67/32;C07C69/618;C07C201/00;C07C201/12;C07C205/56;C07C227/00;C07C227/10;C07C229/44;C07D295/10;C07D295/14 主分类号 C07B61/00
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