Method for the preparation of omega-lactams and their lactamizable precursors
    2.
    发明授权
    Method for the preparation of omega-lactams and their lactamizable precursors 失效
    制备欧米茄及其可乳化前体的方法

    公开(公告)号:US3733317A

    公开(公告)日:1973-05-15

    申请号:US3733317D

    申请日:1970-06-30

    Applicant: SNIA VISCOSA

    Inventor: GIUFFRE L SIOLI G

    CPC classification number: C07D201/10

    Abstract: THERE IS DESCRIBED A PROCESS FOR THE PREPARATION OF OMEGA-LACTAMS HAVING THE GENERAL FORMULA:

    O=C
    WHEREIN N= FROM 2 TO 13, AND/OR OF THEIR LACTAMIZABLE PRECURSORS, WHICH MAY BE CYCLOALIPHATIC OXIMES OR CYCLOALIPHATIC NITROSO DERIVATIVES, MONOMERS OR DIMERS CHARACTERIZED BY THE FACT THAT THE CORRESPONDING CYCLOMETHYLENE KETENE, HAVING THE GENERAL FORMULA

    O=C=C
    WHERE N HAS THE AFOREMENTIONED VALUE, IS SUBJECTED TO NITROSATION WITH A NITROSATING AGENT OF THE FORMULLA NOX, WHERE X CAN BE -HSOBJ4, -CL, -NO2, -OR (IN WHICH R INDICATES AN ALKYL OR ARYL ORGANIC SUBSTITUENT), AT A TEMPERATURE COMPRISED BETWEEN -60*C. AND + 100*C.

    METHOD FOR THE PREPARATION OF PURE LACTAM FROM ITS PRIMARY SOLUTIONS IN AN ORGANIC SOLVENT

    公开(公告)号:IN139022B

    公开(公告)日:1976-04-24

    申请号:IN1514CA1973

    申请日:1973-06-28

    Applicant: SNIA VISCOSA

    Abstract: 1430949 Lactams SNIA VISCOSA SOC NAZIONALE INDUSTRIA APPLICAZIONI VISCOSA SpA 27 June 1973 [28 June 1972] 30468/73 Heading C2C A lactam, e.g. caprolactam, is removed from solution in an organic first solvent by adding to the solution a second solvent which is miscible with the first solvent but which is not a solvent for the lactam so that the lactam is displaced from solution in the first solvent. Exemplified as the first solvent is a phenol containing at least one alkyl substituent which contains 3 or more carbon atoms and has a solubility in water of less than 0À5 g. per 100 g. of water at 25‹ C. and in sulphuric acid solution containing 50 g. of sulphuric acid per 50 g. of water has a solubility of less than 0À2 g. per 100 g. of acid solution at 25‹ C, the substituent groups of the phenol not hindering the activity of the OH group of the phenol. The second solvent may be an aliphatic, aromatic or chlorinated hydrocarbon. A third solvent, e.g. water which is immiscible with both the first and second solvents but which is a solvent for the lactam may also be added to the solution so that the displaced lactam forms a solution in the third solvent.

    4.
    发明专利
    未知

    公开(公告)号:SE7602498L

    公开(公告)日:1976-02-26

    申请号:SE7602498

    申请日:1976-02-26

    Applicant: SNIA VISCOSA

    Abstract: A method for the preparation of omega lactams is disclosed, more particularly epsilon caprolactam or a precursor thereof (such as cyclohexanone oxime), using as the starting material a cyclomethylene ketene, with the simultaneous formation of side products such as cyclohexanecarboxylic acid, wherein an adduct is preliminarly formed between cyclomethylene ketene and sulphur dioxide. The adduct is then reacted with a nitrosating agent so as to obtain, under the appropriate reaction conditions, the expected lactam, more specifically epsilon caprolactam.

    METHOD FOR THE PREPARATION OF PURE LACTAM FROM ITS PRIMARY SOLUTIONS IN AN ORGANIC SOLVENT

    公开(公告)号:ZA734341B

    公开(公告)日:1974-05-29

    申请号:ZA734341

    申请日:1973-06-26

    Applicant: SNIA VISCOSA

    Abstract: 1430949 Lactams SNIA VISCOSA SOC NAZIONALE INDUSTRIA APPLICAZIONI VISCOSA SpA 27 June 1973 [28 June 1972] 30468/73 Heading C2C A lactam, e.g. caprolactam, is removed from solution in an organic first solvent by adding to the solution a second solvent which is miscible with the first solvent but which is not a solvent for the lactam so that the lactam is displaced from solution in the first solvent. Exemplified as the first solvent is a phenol containing at least one alkyl substituent which contains 3 or more carbon atoms and has a solubility in water of less than 0À5 g. per 100 g. of water at 25‹ C. and in sulphuric acid solution containing 50 g. of sulphuric acid per 50 g. of water has a solubility of less than 0À2 g. per 100 g. of acid solution at 25‹ C, the substituent groups of the phenol not hindering the activity of the OH group of the phenol. The second solvent may be an aliphatic, aromatic or chlorinated hydrocarbon. A third solvent, e.g. water which is immiscible with both the first and second solvents but which is a solvent for the lactam may also be added to the solution so that the displaced lactam forms a solution in the third solvent.

    PROCESS FOR OBTAINING PURE LACTAM FROM PRIMARY SOLUTIONS IN AN ORGANIC SOLVENT

    公开(公告)号:YU173673A

    公开(公告)日:1982-02-28

    申请号:YU173673

    申请日:1973-06-27

    Applicant: SNIA VISCOSA

    Abstract: 1430949 Lactams SNIA VISCOSA SOC NAZIONALE INDUSTRIA APPLICAZIONI VISCOSA SpA 27 June 1973 [28 June 1972] 30468/73 Heading C2C A lactam, e.g. caprolactam, is removed from solution in an organic first solvent by adding to the solution a second solvent which is miscible with the first solvent but which is not a solvent for the lactam so that the lactam is displaced from solution in the first solvent. Exemplified as the first solvent is a phenol containing at least one alkyl substituent which contains 3 or more carbon atoms and has a solubility in water of less than 0À5 g. per 100 g. of water at 25‹ C. and in sulphuric acid solution containing 50 g. of sulphuric acid per 50 g. of water has a solubility of less than 0À2 g. per 100 g. of acid solution at 25‹ C, the substituent groups of the phenol not hindering the activity of the OH group of the phenol. The second solvent may be an aliphatic, aromatic or chlorinated hydrocarbon. A third solvent, e.g. water which is immiscible with both the first and second solvents but which is a solvent for the lactam may also be added to the solution so that the displaced lactam forms a solution in the third solvent.

    10.
    发明专利
    未知

    公开(公告)号:NO134150C

    公开(公告)日:1976-08-25

    申请号:NO65171

    申请日:1971-02-23

    Applicant: SNIA VISCOSA

    Abstract: A method is disclosed for the preparation of alicyclic ketenes, useful as intermediates in the preparation of lactams. The instant method consists in a heat treatment of an alicyclic acid, or its anhydride, in a matallic reactor exempt from nickel, at high temperatures but under subatmospherical pressures. A catalyst of the type XP(OR)3 wherein X is selected from the group consisting of oxygen, sulphur and selenium and R is an alkyl radical is preferred for accelerating the reactions. The temperatures are in the range from 550 DEG to 750 DEG C and the preferred pressure is under 100 millimeters of mercury. High yields and conversion rates are obtained and the purity of the end product is more than satisfactory. The method can be applied to the preparation of a number of alicyclic ketenes.

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