公开(公告)号：US20130303702A1

公开(公告)日：2013-11-14

申请号：US13866474

申请日：2013-04-19

Applicant: BASF SE

Inventor： Michael Krayer ,  Joachim Schmidt-Leithoff ,  Kevin Neigh ,  Karl Matos

IPC: C08F291/00 ,  C08G73/02 ,  C08G77/38

CPC classification number: C08F291/00 ,  C08G73/0233 ,  C08G77/38 ,  C08J7/16 ,  C08K5/0025 ,  C08K5/55

Abstract: The present invention relates to a process for the modification of a polymer surface. The polymer surface is treated with (i) an organoborane-amine complex and subsequently with (ii) a radically polymerizable monomer compound and optionally a deblocking agent.

Abstract translation: 本发明涉及一种改性聚合物表面的方法。 聚合物表面用（i）有机硼烷 - 胺络合物处理，随后与（ii）可自由基聚合的单体化合物和任选的去封闭剂一起处理。

公开(公告)号：US20130109876A1

公开(公告)日：2013-05-02

申请号：US13661811

申请日：2012-10-26

Applicant: BASF SE

Inventor： Stefan Pichlmair ,  Joachim Schmidt-Leithoff

IPC: C07F3/06

CPC classification number: C07F3/06

Abstract: The present invention relates to a process for the preparation of organozinc halides with low residual alkyl or aryl halide content.

Abstract translation: 本发明涉及制备具有低残留烷基或芳基卤含量的有机卤化锌的方法。

公开(公告)号：US09988331B2

公开(公告)日：2018-06-05

申请号：US13658003

申请日：2012-10-23

Applicant: BASF SE

Inventor： Gunnar Heydrich ,  Gabriele Gralla ,  Matthias Rauls ,  Joachim Schmidt-Leithoff ,  Klaus Ebel ,  Wolfgang Krause ,  Steffen Oehlenschläger ,  Christoph Jäkel ,  Marko Friedrich ,  Eike Johannes Bergner ,  Nawid Kashani-Shirazi ,  Rocco Paciello

IPC: C07C29/56 ,  C07C29/17 ,  C07C29/78 ,  C07C45/62 ,  C07C45/82

CPC classification number: C07C29/56 ,  C07B2200/07 ,  C07C29/172 ,  C07C29/78 ,  C07C45/62 ,  C07C45/82 ,  C07C2601/14 ,  C07C2601/16 ,  C07C47/21 ,  C07C35/12 ,  C07C35/17

Abstract: The present invention relates to a particularly economic overall method for producing menthol, specifically for producing optically active, essentially enantiomerically and diastereomerically pure L-menthol and racemic menthol, starting from the starting material citral which is available inexpensively on an industrial scale. The method has the following steps a.1) catalytic hydrogenation of neral and/or geranial to give citronellal, b.1) cyclization of citronellal to isopulegol in the presence of an acidic catalyst, c.1) purification of isopulegol by crystallization and d.1) catalytic hydrogenation of isopulegol to give menthol.