Basf Aktiengesellschaft

Peter Lechtken

Hubert Trauth

Ingolf Buethe

Gerhard Hoffmann

Albert Hettche

Dieter Hermeling

Bernd Bronstert

Anton Hesse

John Lynch

Stefan Weiss

Axel Nuerrenbach

Manfred Jacobi

Rudolf Vyvial

Werner Trimborn

Ulrich Hoercher

Juergen Schole

Peter Bassler

Hardo Siegel

Randolf Hugo

Wilhelm Weber

Gustav Bock

Michael Horner

Peter Hammes

Friedrich Sauer

Dankmar Scholz

Klaus Schmieder

Peter Paul Hoppe

Gerhard Mueller

Hubert Tiefenbacher

Matthias Fankhaenel

Barbara Jessel

Walter Kohler

Peter Kutschera

Walter Nicolaus

Triphenylphosphine (TPP) is prepared by reacting triphenylphosphine dichloride (TPPCl.sub.2) with magnesium, aluminum and/or iron in the presence of an inert solvent, employing a TPPCl.sub.2 solution whose content of phosgene, chlorine, diphosgene, hydrogen chloride, thionyl chloride, sulfuryl chloride, phosphorus trichloride, phosphorus oxychloride and/or aliphatic halogen compounds (active chlorine compounds) totals less than 1000 ppm Cl.

Preparation of triphenylphosphine

A process for isolating triphenylphosphine (TPP) from a triphenylphosphine/aluminum chloride complex dissolved in chlorobenzene by decomplexation, hydrolysis and extraction using water and subsequent separation of the liquid/liquid dispersion, which is composed of a TPP-containing chlorobenzene phase and of an containing Al and Cl compounds aqueous phase, into a TPP-containing chlorobenzene phase and into a TPP-free, aqueous phase, containing Al and Cl compounds, wherein water is dispersed in the chlorobenzene phase in a ratio of 0.6-0.95 kg of water per kg of chlorobenzene solution in a 1st mixing apparatus in such a way that the temperature resulting from the hydrolysis is in the range from 60.degree. to 90.degree. C., the dispersion being carried out with residence times of 5-30 minutes and energy densities of 2-10 kW/m.sup.3, a second dispersion is carried out in a 2nd mixing apparatus with residence times of 5-60 minutes and energy densities of 0.05-0.5 kW/m.sup.3, and the heavier TPP-containing chlorobenzene phase is separated from the lighter TPP-free, aqueous phase containing Al and Cl compounds in a phase separator.

Isolation of triphenylphosphine

Undesirable odors are removed from fatty ester mixtures which, in addition to other components, contain the esters of highly unsaturated fatty acids, in particular of highly unsaturated 3-fatty acids, such as eicosapentaenoic acid or docosahexaenoic acid, by a process in which the fatty ester mixture is treated with a complex hydride, in particular with sodium borohydride solution. The process is particularly suitable for removing undesirable odors from fatty ester mixtures obtained from fish oil, for example by transesterification with an alkanol of 1 to 3 carbon atoms.

Deodorization of fatty ester mixtures

Textile materials made of polyester, triacetate, acetate or polyamide or mixtures thereof are printed by the discharge printing or discharge resist printing technique by using as discharging agent for disperse dyes a 3-aminoreductone of the formula ##STR1## where R.sup.1, R.sup.2 and R.sup.3 are identical or different and each is hydrogen, methyl or ethyl and R.sup.4 is linear or branched alkyl or alkenyl of from 1 to 20 carbon atoms, which may be monosubstituted or polysubstituted by hydroxyl, alkoxy of from 1 to 3 carbon atoms in the alkyl or acetoxy, or is a radical --(CH.sub.2 --CH.sub.2 --O).sub.n H where n is from 1 to 10 and which may be etherified with alkyl of from 1 to 3 carbon atoms or esterified with acetyl, or R.sup.4 together with the N-atom is the radical of an aliphatic .alpha.- or .beta.-amino acid of from 2 to 15 carbon atoms, in which case the carboxyl group may be present in neutralized form as an alkali metal, alkaline earth metal or ammonium salt or in esterified form as a C.sub.1 -c.sub.10 -alkyl ester, or a mineral acid salt thereof.

Discharge and discharge resist printing using aminoreductones

d-.alpha.-Tocopherol is prepared from a mixture obtained from natural intermediates and containing .alpha.-, .beta.-, .gamma.- and .delta.-tocopherols, by methylation at the aromatic ring of the tocopherols by reaction with formaldehyde or with a compound which donates formaldehyde under the reaction conditions, and subsequent catalytic hydrogenation, by a process in which the reaction with formaldehyde or with the formaldehyde donor is carried out at from 150.degree. to 200.degree. C. in the presence of an alkyl ester of phosphoric or phosphorous acid.

Preparation of d-.alpha.-tocopherol from natural intermediates

Stabilizer mixtures for stabilizing plastics comprising one part by weight of a chroman derivative (I) of the general formula ##STR1## where R= ##STR2## where Z=C.sub.7 -C.sub.30 -alkyl, --CH.sub.2 CH.sub.2 --S--[C.sub.1 -C.sub.30 -alkyl] or ##STR3## and from 5 to 14 parts by weight of an organic phosphite of the general formula (II) ##STR4## where R.sup.1, R.sup.2 and R.sup.3 are identical of different alkyl and/or aryl or of an organic phosphonite of the formula (III) ##STR5## where +is C(CH.sub.3).sub.3, a mixing ratio (a):(b) of from 1:6 to 1:10 being preferred.

Stabilizer mixtures for plastics

Acylphosphine oxide compounds of the general formula ##STR1## where R.sup.1 is alkyl, cyclohexyl, cyclopentyl, aryl which is unsubstituted or substituted by halogen, alkyl or alkoxy, or an S-containing or N-containing five-membered or six-membered heterocyclic radical,

Photocurable compositions with acylphosphine oxide photoinitiator

Stabilizers consisting of (a) 2,5,7,8-tetramethyl-2-(2'-stearyloxyethyl)-chroman and (b) glyceryl stearate, glyceryl hydroxystearate, partial esters of stearic acid with condensates of glycerol and trimethylolpropane, triglyceryl stearate and/or tetraglyceryl stearate, with or without further conventional additives, the weight ratio of (a) to (b) being from 10:1 to 1:10, give improved stabilization to discoloration and superior stability during processing when used in plastics such as polyethylene or polypropylene.

Stabilizers

2,3-Dihydrobenz-4-oxa-1-thiins of the general formula I ##STR1## where R.sup.1, R.sup.2 and R.sup.3 are each hydrogen, methyl or methoxy, and R.sup.2 and R.sup.3 together may furthermore be a fused benzene ring, R.sup.4 is hydrogen or an m-valent aliphatic hydrocarbon radical which may be interrupted by sulfur and /or carry thiol groups as substituents, or is halogen when n is zero, X is --O--, --S-- or --O--CO--, m is 1 or 2 and n is zero or 1, are useful as antioxidants for organic materials.

Polypropylene stabilizing anti-oxidant 2,3-dihydrobenz-4-oxa-1-thiin

A growth-promoting additive for feeds consists of a commercial growth promoter as well as an aminoreductone of the formula ##STR1## where R.sup.1, R.sup.2 and R.sup.3 are each hydrogen, methyl or ethyl and R.sup.4 is an unsubstituted or substituted C.sub.1 -C.sub.20 -alkyl or alkenyl radical or a radical of an aminoacid.

Mixtures which promote growth and increase production, and feeds and

Organic materials which contain from 0.001 to 10% by weight of an aminoreductone I ##STR1## where R.sup.1, R.sup.2 and R.sup.3 are H, methyl or ethyl and R.sup.4 is the radical of a naturally occurring .alpha.- or .beta.-aminoacid or of a C.sub.1 -C.sub.10 -alkyl ester thereof or, in the case of an .alpha.-aminoacid, a lactone having a 2--OH group in the cyclohexenone ring, or R.sup.4 is C.sub.1 -C.sub.20 -alkyl which is unsubstituted or substituted by --OH, C.sub.1 -C.sub.4 -alkoxy or C.sub.1 -C.sub.4 -acyloxy, or is --(CH.sub.2 --CH.sub.2 --O).sub.n H, which may be etherified with a C.sub.1 -C.sub.4 -alkanol or esterified with a C.sub.1 -C.sub.4 -fatty acid, and where n is from 2 to 10, or a mineral salt thereof. Novel compounds Ia differ from I in having the radical R.sup.4a, where R.sup.4a is R.sup.4 with the exception of methyl. Compounds I are prepared by reacting the corresponding 2,3-dihydroxycyclohex-2-en-1-one with an amine HN(R.sup.3)R.sup.4 or a mineral acid salt thereof.

Aminoreductones

Animal feeds and drinks containing small amounts of compounds of the formula Ia or Ib ##STR1## where R.sup.1 is hydrogen, low molecular weight alkyl or alkoxy, or halogen, R.sup.2 is hydrogen or low molecular weight alkyl and R.sup.3 and R.sup.4 are hydrogen or a low molecular weight aliphatic or araliphatic radical. The compounds of the formulae Ia and Ib promote growth without exerting an antibiotic action.

Growth-promoting feed and drink

A photopolymerizable recording composition which comprises a mixture, containing a photoinitiator, of (a) a photopolymerizable olefinically unsaturated monomer and (b) an organic polymeric binder, wherein the photoinitiator is an acylphosphine oxide compound of the formula R.sup.1 R.sup.2 PO--CO--R.sup.3, where R.sup.1 and R.sup.2 are certain organic radicals and R.sup.3 is tert.-alkyl or a cyclic radical with two substituents in the ortho-position to the carbonyl group. The recording compositions have a high reactivity when irradiated with UV light and are used in particular for the preparation of printing plates, relief plates and photo-resists.

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Frankenthal, Germany

Peter Lechtken