31.
    发明专利
    未知

    公开(公告)号:DE59404482D1

    公开(公告)日:1997-12-04

    申请号:DE59404482

    申请日:1994-08-19

    Applicant: BASF AG

    Abstract: N-alkenylcarboxylic acid amides of formula HR C=CRN(R )C(O)R (I) are prepd. from carboxylic acid alkenyl esters of formula HR C=CR OC(O)R (II) and a carboxamide of formula HNR NC(O)R (III), by reaction in presence of a base. In formulae, R = one is H and the other is H or 1-4 C alkyl; R = (cyclo)aliphatic, araliphatic or aromatic gp., which may form a 3-10-member bridge with R ; R = H, or a (cyclo)aliphatic or aromatic gp.; and R = H or a (cyclo)aliphatic or aromatic gp. Pref. N-vinylpyrrolidone or N-vinylcaprolactam are prepd. Reaction is at 20-80 degrees C, without a solvent, using a tert. amine or Na methylate, K tert.butylate or K2CO3 as base. The amt. of base is 0.2-1 equivs. w.r.t. 1 equiv. of amide (III).

    Preparation of alkoxy-silane compounds containing vinyl ether groups

    公开(公告)号:DE19649998A1

    公开(公告)日:1997-06-19

    申请号:DE19649998

    申请日:1996-12-03

    Applicant: BASF AG

    Abstract: The preparation of compounds of formula CH2=CH-O-X-CH2CH2SiRy(OR')3-y (I) comprises reacting divinyl ethers of formula CH2=CH-O-X-CH=CH2 (II) with silanes of formula HSiRy(OR')3-y (III) at 70 - 150 deg C in the presence of a homogeneous hydrosilation catalyst. The catalyst is a platinum or rhodium compound, and the amount of Rh or Pt is 0.05 - 10 ppm with respect to (II and (III). R, R' = 1-6C alkyl or 6-10C aryl; X = 1-20C hydrocarbon, optionally substituted by halo and/or containing O atoms; and y = 0 - 2.

    33.
    发明专利
    未知

    公开(公告)号:DE19509362A1

    公开(公告)日:1996-09-19

    申请号:DE19509362

    申请日:1995-03-15

    Applicant: BASF AG

    Abstract: Prepn. of N-vinyl-lactams (I) of formula (A) (where R = CH=CH2; n=1-3) comprises reacting lactams (II) of formula (A) (where R = H; n = 1-3) with (a) 10-90 wt.% aq. alkali hydroxide soln. by distn. at 50-250 degrees C and 1-100 mbar with a residence time of 0.1-5 hrs. and then (b) C2H2 at 60-250 degrees C and 1-100 bar. Pref. reaction (a) is carried out in a column with at least 2 theoretical plates. (II) and aq. alkali hydroxide soln. are fed into the upper third of the column. A 30-60, esp. 45-55 wt.% soln., more esp. KOH soln., is used. Reaction is carried out at 70-180 degrees C and 1-30 mbar with a residence time of 0.5-2 hrs.

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