Basf Aktiengesellschaft

Marc Heider

Jochem Henkelmann

Thomas Ruhl

Martin Schmidt-Radde

Michael Karcher

Bernd Wenderoth

Bernd Lothar Marczinke

Dieter Littmann

Harald Rust

Roger G Klimesch

Knut Oppenlander

Albrecht Dams

Hans-Joachim Muller

Albin Berger

Heinrich Hartmann

Walter Denzinger

Peter Zehner

Birgit Potthoff-Karl

Hans-Juergen Raubenheimer

Thomas Preiss

Arthur Hohn

Ralf-Thomas Rahn

Herbert Helfert

Susanne Stutz

Peter Hofmann

Heinz Rutter

Karl-Heinz Buechner

Klaus Bittins

Martin Schafer

Thomas Ruehl

Stefan Berg

Jochen Kellenbenz

Bernd Fiechter

Kurt Josef Wagner

Butyrolactone-preparation process

Preparation of vinyl carbamates

Ethylene-based copolymers which are suitable as flow improvers for mineral oil middle distillates are composed of

Ethylene-based copolymers and their use as flow improvers in mineral oil

Water-soluble, carboxyl-containing copolymers, the preparation thereof

A process for preparing N-alkenylureas of the general formula I ##STR1## where R.sup.1 and R.sup.2 are hydrogen, C.sub.1 - to C.sub.40 -alkyl, C.sub.2 - to C.sub.40 -alkenyl, C.sub.3 - to C.sub.20 -cycloalkyl, C.sub.4 - to C.sub.20 -alkylcyc1oalkyl, C.sub.4 - to C.sub.20 -cycloalkylalkyl, aryl, C.sub.7 - to C.sub.20 -alkylaryl or C.sub.7 - to C.sub.20 -aralkyl, or aryl, C.sub.7 - to C.sub.20 -alkylaryl or C.sub.7 - to C.sub.20 -aralkyl which are mono- to pentasubstituted by C.sub.1 - to C.sub.8 -alkyl, C.sub.1 - to C.sub.8 -alkoxy or halogen, together are a C.sub.2 - to C.sub.10 -alkylene chain which is unsubstituted or mono- to hexasubstituted by C.sub.1 - to C.sub.8 -alkyl, and

Preparation of N-alkenylureas

Process for carrying out gas/liquid reactions at from (-50.degree.) to 300.degree. C. and from 0.1 to 100 bar by carrying out the reaction in the absence of a continuous gas phase, and, as a special case, a process for the batchwise reaction of acetylene in the liquid phase at from 0.degree. to 300.degree. C. and from 2 to 30 bar, in which acetylene is introduced a) in the absence of a continuous gas phase and b) under isobaric conditions to a degree of saturation of from 5 to 100%.

Process for carrying out gas/liquid reactions under avoidance of a

Acetylenic compounds of the general formula I

Preparation of acetylenic compounds

The preparation of monovinyl ethers of the general formula I ##STR1## in which A stands for a chemical bond or for a methylene or ethylene group, the radicals R.sup.1 and R.sup.2 independently stand for hydrogen, alkyl, cycloalkyl, or aryl groups or R.sup.1 and R.sup.2 together form a C.sub.3 -C.sub.5 alkylene bridging member, by the reaction of a diol of the general formula II ##STR2## in which the variables have the above meanings, with acetylene in the presence of a base, in which the reaction is carried out at 150.degree.-250.degree. C. under an acetylene partial pressure of 5-25 bar until 40-80% of the diol has been converted, at which point the reaction is stopped and the monovinyl ether of the formula I is isolated.

Preparation of monovinyl ethers

Preparation of N-alkenyl carboxamides of the general formula I ##STR1## in which the radicals R.sup.1 to R.sup.4 independently stand for hydrogen or for aliphatic, cycloaliphatic, or aromatic radicals, which optionally carry inert substituents, wherein an amide of the general formula II ##STR2## in which the radical R.sup.1 has the above meaning, and a carbonyl compound of the general formula III ##STR3## in which the radicals R.sup.2 to R.sup.4 have the above meanings, are caused to react in the presence of a base, said reaction being either

Preparation of N-alkenyl carboxamides

Oxime ethers of the general formula I ##STR1## where the variables have the following meanings: R.sup.1, R.sup.2 independently of one another hydrogen, C.sub.1 -C.sub.20 -alkyl, C.sub.4 -C.sub.10 -cycloalkyl, C.sub.6 -C.sub.10 -aryl or together a bridge of 3-14 carbon atoms,

Copolymerizable oxime ethers

Preparation of a monolithium acetylide/ammonia complex by the reaction of lithium amide and acetylene in ammonia, by carrying out the reaction at a temperature of from -10.degree. to 30.degree. C.

Preparation of a monolithium acetylide/ammonia complex

Reaction mixtures obtained in addition reactions of OH-- or NH-- carrying compounds with acetylene or propyne in the presence of alkali metal alcoholates or alkali metal amides are worked up by distilling off the vaporizable components from the reaction mixture in a thin-film evaporator. Before removal of the vaporizable components from the reaction mixture, a particularly defined polyether is added thereto.

Working up reaction mixtures obtained in addition reactions with

N-Vinyllactams of the general formula I ##STR1## where n is from 1 to 3, are prepared by a process which comprises reaction of a lactam of the general formula II ##STR2## where n is from 1 to 3, with from 10 to 90 percent by weight of an aqueous alkali metal hydroxide solution with distillation at from 50.degree. to 250.degree. C. and from 1 to 100 mbar and with a residence time of from 0.1 to 5 hours and subsequent reaction with acetylene at from 60.degree. to 250.degree. C. and from 1 to 100 bar.

Preparation of n-vinyllactams

N-Alkenylcarboxamides of the formula I ##STR1## where at least one of the radicals R.sup.1 is hydrogen, the second radical R.sup.1 is hydrogen or C.sub.1 -C.sub.4 -alkyl and R.sup.2 is hydrogen or an aliphatic, cycloaliphatic or aromatic radical, are prepared by reacting an alkenyl carboxylate of the formula II ##STR2## where R.sup.1 has the abovementioned meanings and R.sup.3 is hydrogen or an aliphatic, cycloaliphatic or aromatic radical, and a carboxamide of the general formula III ##STR3## where R.sup.2 has the abovementioned meanings, in the presence of a base.

Preparation of N-alkenylcarboxamides

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Marc Heider