Translation of "Weiterreagieren" in English

The suspension formed thereby was allowed to react further under reflux conditions.

The mixture is then left at +7° C. to react further slowly.

The mixture is then further reacted at that temperature for 2 hours.

The mixture is then further reacted for 27 hours at that temperature.

The peroxyl radical (RHO2•), for instance,may also continue its reaction as follows:

The mixture was warmed to room temperature and left to react for 1 hour.

This group can (in part) react further with additional isocyanate groups to obtain a uretonimine group.

The cyclododecadienone target product can react further with further dinitrogen monoxide to give diketones.

Thereafter, the mixture was left to react further at 81° C. for another 1 hour.

The first product is imidazolides, and these are then further reacted intermolecularly to give the polycarbonates.

After that, the reaction is allowed to continue for one hour at room temperature.

These intermediate products are instable at high temperatures and undergo further reactions.

The reaction mixture is then allowed to come to room temperature and to react further for about 30 minutes.

The stabilizer is obviously unable to continue reacting through the polyadduct covering already formed.

The desired product IPA can also react further with elimination of water b) to form the undesired diisopropyl ether (DIPE).

The batch is allowed to react at room temperature until the isocyanate content has reached 6.6%.

Now the reaction mixture is allowed to continue to react for 4 h at 40° C. while stirring it.

Now the reaction mixture is allowed to continue to react for 4 h at 40° C. while stirring it.

The R3Si–NH–SiR3 forms R3Si–NH2 and HO–SiR3 which can further react (condensation) to form R3Si–O–SiR3 (siloxanes).

There are preferably used those resins which do not react further chemically when exposed to air or with themselves and possibly crosslink.

When these products are incorporated into polymers, the free hydroxyl groups can further react by known reactions, so that specific, modified plastics can be obtained.

They are compounds of melamine and formaldehyde which are formed in an anhydrous solvent having at least two alcoholic hydroxyl groups, for example, ethylene glycol, and/or react further with the solvent in a simple manner.

Furthermore, it is surprising that the intermediate products, of the formula (VI), from the first reaction stage of the process according to the invention react further in an unambiguous manner to give the end product of the formula (VII) according to the invention, in spite of the cis/trans isomerism made possible by the double bond.

In addition, they cannot react further or cross-link, either with themselves or with the elastomeric or acrylate component, once the emulsion or dispersion has been produced, as they lack the necessary chemical groups.

After the addition of trimethylol propane, the mixture is left to react at the same temperature until it has an isocyanate content of 4.9%.

The technical difficulty of obtaining high yields of phosphoric acid triesters by the Schotten-Baumann reaction lies in the fact that the phosphorus oxychloride generally used is partly or completely hydrolysed by the aqueous sodium hydroxide and the sodium salts of the corresponding hydroxy compounds thus formed do not further react with the aromatic hydroxy compounds under the reaction conditions applied to form the phosphoric acid ester.