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    • 8. 发明专利
    • PURIFICATION OF 2CYANOACRYLATE
    • JPH10265448A
    • 1998-10-06
    • JP7121297
    • 1997-03-25
    • MITSUBISHI CHEM CORP
    • OTA TAKAYUKINOGUCHI HIROSHI
    • C07C253/34C07C255/23C09J4/04
    • PROBLEM TO BE SOLVED: To efficiently obtain the subject compound useful for medical adhesives, etc., by treating impurities such as reaction materials used in a synthetic process and the resultant by-products by separation, etc., using a specific organic solvent. SOLUTION: A saturated hydrocarbon organic solvent having 6.5-8.5 solubility parameter, e.g. C5 H12 or C6 H14 , using usually in an amount of 1-20 pts.wt., preferably 2-5 pts.wt. based on 1 pt.wt. crude compound of a compound represented by the formula CH2 = C(CN)COOR (R is an 8-20C hydrocarbon group) is added to the crude compound and both components are sufficiently stirred and as necessary, the mixture is allowed to stand for about 10-200 min under ice-chilled conditions to sufficiently subject the reaction product to phase separation. The separated undissolved material is preparedly distilled under reduced pressure at a low temperature to provide 2-cyanoacrylate in high purity. The compound of the formula is obtained by reacting isobutly cyanoacrylate with anthracene, hydrolyzing the reaction product under basic conditions, acidifying the reaction solution to afford 2-cyanoacrylic acid, then, changing the 2- cyanoacrylic acid to corresponding acid chloride, reacting the acid chloride with an alcohol and reacting the reaction product with a stroingly acidic dienophile.