Preparation of (2-cyanoethyl) ketones
    1.
    发明授权
    Preparation of (2-cyanoethyl) ketones 失效
    (2-氰基乙基)酮的制备

    公开(公告)号:US3686262A

    公开(公告)日:1972-08-22

    申请号:US3686262D

    申请日:1970-09-15

    Applicant: STAMICARBON

    CPC classification number: C07C255/00

    Abstract: A PROCESS FOR THE PREPARATION OF (2-CYANOETHYL) KETONES BY THE HYDROLYSIS OF THE CORRESPONDING (2-CYANOETHYL)-N-SUBSITUTED KETOIMINE WITH THE SUBSEQUENT RECOVERY OF A PRIMARY AMINE, THE PRIMARY AMINE BOILING AT A LOWER TEMPERATURE THAN WATER AND/OR FORMING WITH WATER AN AZEOTROPE BOILING AT A LOWER TEMPERATURE THAN WATER AND CARRYING ON ITS NITROGEN ATOM THE SAME GROUP AS THAT OF THE NITROGEN ATOM OF THE CORRESPONDING KETOIMINE IS DISCLOSED. WHEN THE RESULTING KETONE IS 5-CYANOPENTANONE-2 THIS MAY BE USED AS A STARTING PRODUCT FOR THE PREPARATION OF A-PIPECOLINE.

    PROCESS FOR THE PREPARATION OF PIPERIDINES

    公开(公告)号:CA952529A

    公开(公告)日:1974-08-06

    申请号:CA107571

    申请日:1971-03-12

    Applicant: STAMICARBON

    Abstract: 1327335 Process for making piperidines STAMICARBON NV 19 April 1971 [12 March 1970] 23823/71 Heading C2C The invention comprises hydrogenating an N-substituted-4-cyanoaldimine, optionally in the presence of ammonia and a solvent, to afford piperidine or a C-substituted piperidine and a primary amine carrying the same substituent on the N-atom as is present on the N-atom of the aldimine. The examples describe the conversion of: N-cyclohexyl-4-cyano-2,2- dimethylbutyraldimine to 3,3-dimethylpiperidine, cyclohexylamine and 1,5-diamino-2,2-dimethylpentane; N - hexyl - 4 - cyano - 2,2 - dimethylbutyraldimine to 3,3-dimethylpiperidine, hexylamine and 1,5 - diamino - 2,2 - dimethylpentane; N - cyclohexyl - 4 - cyanobutyraldimine to piperidine, cyclohexylamine and 1,5-diaminopentane; N - cyclohexyl - 4 - cyano - 2 - ethyl - butyraldimine to 3 - ethyl - piperidine, cyclohexylamine and 2-ethyl-1,5-diaminopentane; N - hexyl - 2,2 - dimethyl - 4 - cyanobutyraldimine to 3,3 - dimethylpiperidine, 1 - hexyl - 3,3 - dimethylpiperidine and hexylamine; and N-cyclohexyl-4-cyano-2-propylbutyraldimine to 3-propylpiperidine, cyclohexylamine and 1-cyclohexyl-3-propylpiperidine

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