Extracting cyclohexene from mixts. with benzene and/or cyclohexane

    公开(公告)号:DE4002764A1

    公开(公告)日:1991-08-01

    申请号:DE4002764

    申请日:1990-01-31

    Applicant: BASF AG

    Abstract: Cyclohexane (I) is produced from mixts. of (I) with benzene and/or cyclohexane by (a) reaction of anthracene (II) (opt. contg. inert substits.) with (I) in the mixt. to form an adduct of (I) and (II), (b) sepg. the addn. prod. from the mixt. and (c) decomposing the addn. prod. to produce (I) and (II) by heating at 150-500 deg.C. Amt. of (II) used is 1-30 mol/mol. (I), stage (a) is carried out at 100-300 deg.C and 10-300 bar, (II) is substd. with up to two 1-4C alkyl gps., temp. in stage (c) is 200-400 deg.C. Typical mixts. contain 10-40 wt.% (I), 1-50 wt.% cyclohexane and 10-90 wt.% benzene, suitable substd. (II) are e.g. 2- or 9-methyl-(II), 9-ethyl-(II), 9-chloro-(II), 9-cyano-(II) etc., adduct is sepd. by crystallisation and filtration or by distillation of benzene and cyclohexane and decomposed at 200-400 deg.C and 0.1-10 bars.

    45.
    发明专利
    未知

    公开(公告)号:DE3843793A1

    公开(公告)日:1990-07-05

    申请号:DE3843793

    申请日:1988-12-24

    Applicant: BASF AG

    Abstract: Caprolactam is prepared by heating a 6-aminocaproic ester in liquid phase in the presence of water to 230 DEG -350 DEG C. under superatmospheric pressure in a reaction medium comprising a liquid aromatic hydrocarbon having a boiling point of from 80 DEG to 240 DEG C. which is inert under reaction conditions, and isolating caprolactam from the reaction mixture.

    PROCESS FOR THE PREPARATION OF 4-MONOACETALS OF 2-METHYL-2-BUTENE-1,4-DIAL

    公开(公告)号:DE3760246D1

    公开(公告)日:1989-07-20

    申请号:DE3760246

    申请日:1987-01-21

    Applicant: BASF AG

    Abstract: 4-Monoacetals of (E)-2-methylbut-2-ene-1,4-dial of the general formula I (I) where R1 and R2 are each an aliphatic hydrocarbon radical of 1 to 12 carbon atoms, cycloalkyl of 5 to 7 carbon atoms or benzyl, or R1 and R2 together form an ethylene or propylene radical which may furthermore be substituted by lower alkyl, are prepared by a process in which a compound of the general formula II (II) where either R3 and R4 are both one of the groups where R1 and R2 have the above meanings, or R3 is one of the groups and R4 is formyl is reacted, at from 20 DEG to 200 DEG C., in the presence of an acidic compound, with the compound of the formula III R5-OH (III) where R5 is hydrogen, alkyl of 1 to 12 carbon atoms or hydroxyalkyl of 2 to 5 carbon atoms, and, where R3 and R4 are each R5 is alkyl, and where R3 and R4 are each R5 is hydrogen, and where R3 is and R4 is R5 is hydrogen and/or alkyl.

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