Basf Aktiengesellschaft

Basfaktiengesellschaft

Basf Se Corporation

Michael Huellmann

Joaquim Henrique Teles

Rainer Becker

Thomas Kuekenhoehner

Matthias Irgang

Karl Siegfried Brenner

Ernst Buschmann

Walter Himmele

Walter Gramlich

Nicolas Vautravers

Marta Reinoso Garcia

Charles Schommer

Lothar Franz

Wolfgang Franzischka

Heinz Eckhardt

Emil Scharf

Gerald Lauterbach

Christof Palm

Herbert Mayr

Hans-Ulrich Scholz

Christiane Brueckner

Josef Gnad

Georgios Dodekatos

Polytetrahydrofuran or C.sub.2 -C.sub.10 -alkylene oxide/tetrahydrofuran copolymers having a molecular weight of from 250 to 20,000 Dalton are prepared by the cationic polymerization of tetrahydrofuran or tetrahydrofuran and C.sub.2 -C.sub.10 -alkylene oxides in the prsence of a promoter by a process in which the catalyst used is a mixture of one or more C.sub.2 -C.sub.6 -di- or tricarboxylic acids with boric acid.

Preparation of polytetrahydrofuran or tetrahydrofuran/alkylene oxide

Preparation of N-(2-hydroxyethyl)-piperazine by reacting triethanolamine with ammonia in the presence of hydrogen at from 100.degree. to 500.degree. C. and from 10 to 500 bar over a heterogeneous catalyst in which the catalytically active material contains from 20 to 85% by weight of ZrO.sub.2 or Al.sub.2 O.sub.3 or mixtures thereof, from 1 to 30% by weight of at least one copper oxide, calculated as CuO, and from 1 to 60% by weight of at least one oxide of cobalt, nickel or molybdenum, calculated as CoO, NiO and MoO.sub.3, respectively.

Preparation of N-(2-hydroxyethyl)-piperazine

Process for the preparation of N-alkenylpyrrolidones of the general formula ##STR1## in which R denotes hydrogen or C.sub.1 -C.sub.20 alkyl, by the reaction of an N-alkylpyrrolidone of the general formula ##STR2## in which R has the aforementioned meanings, and x and Y stand for OH, C.sub.1 -C.sub.20 alkoxy or C.sub.2 -C.sub.20 alkoxycarbonyl, provided that one of the two radicals x and denotes hydrogen, at temperatures ranging from 200.degree. to 600.degree. C. and pressures ranging from 0.1 to 5 bar, wherein the process is carried out in the presence of an acid heterogenous catalyst except for an oxide of a Group IIb, Group IIIb, Group IVb, and Group VIb metal.

Preparation of N-alkenylpyrrolidones

The preparation of 3-arylacrylic acids and their derivatives I ##STR1## where Ar is aryl which can additionally have substituents which do not react with ketene and are stable under the conditions of the reaction described below, and

Preparation of 3-arylacrylic acids and their derivatives

Preparation of vinyl glycols (I) ##STR1## (R.sup.1 to R.sup.6 =H, a carbo-organic radical, optionally substituted) in which an unsaturated diol of formula II ##STR2## is isomerized in the presence of a rhenium catalyst under neutral conditions. The compounds (I) serve as intermediates for the preparation of active substances and for the preparation of polymers.

Preparation of vinyl glycols

Muscone of the formula I ##STR1## is prepared by a process in which an open-chain 2,15-diketone of the general formula II

Preparation of muscone, intermediates for this preparation and

A process for preparing 1,1,3,4,4,6-hexamethyl-1,2,3,4-tetrahydronaphthalene of the formula I ##STR1## comprises reacting p-cymene of the formula II ##STR2## with a hexene of the formula IIIa, IIIb and/or IIIc ##STR3## in the presence of a catalytic amount of aluminum halide and a catalytic amount of a triphenylmethyl compound of the formula IV ##STR4## wherein R.sup.1, R.sup.2 and R.sup.3 are each, independently of one another, hydrogen, C.sub.1 -C.sub.4 -alkyl, nitro or halogen and X is hydrogen or halogen.

Preparation of 1,1,3,4,4,6-hexamethyl-1,2,3,4-tetra-hydronaphthalene

3,9-Dihydroxynonyne and its derivatives protected at the 9-OH function, of the general formula I ##STR1## where R is hydrogen or a conventional alcohol protective group, and processes for the preparation of the compounds I.

3,9-dihydroxynonyne and its derivatives protected at the 9-OH function

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Heppenheim, Germany

Michael Huellmann