Showa Denko K.k.

Showa Denko Kabushiki Kaisha

Showa Denka K.k.

Shawa Denko K.k.

Kuniomi Marumo

Shuichi Sugita

Tetsuo Kudo

Norio Kametaka

Hiroshi Uchida

Toshiyuki Aizawa

Yasuyuki Sakai

Yuseki Suyama

Taketoshi Naito

Kunio Imamura

Yoshimasa Ishimura

Hiroyuki Monzen

Kouhei Morikawa

Motoo Miura

Tsutomu Nozawa

Kazuo Kanbayashi

Noriyuki Suzuki

Shuuji Hirayama

Shigehiro Chaen

Ryoji Ishioka

Hiroshi Yasuda

Makoto Saito

Haruaki Ito

Sumio Soya

Kazuo Sekiguchi

Kimitaka Ohshiro

Kenichiro Maki

Takashi Tani

Tetsuro Fujita

Tutomu Nozawa

Kiyonori Tokuda

A process for producing a cyanobenzoic acid compound, a cyanobenzamide compound, an alkyl cyanobenzoate compound, and a cyanobenzoyl chloride compound, which are useful intermediates for a variety of chemicals such as pharmaceuticals, agrochemicals, liquid crystals, and monomers for functional polymers. One nitrile group of an easily available phthalonitrile compound is selectively hydrolyzed to thereby produce a cyanobenzamide compound with high selectivity and yield. The cyanobenzamide compound thus-produced is transformed under acidic conditions into a cyanobenzoic acid compound and a cyanobenzoate ester compound without the cyano group of the benzene ring being damaged.

Process for producing cyanobenzoic acid derivatives

Noble metal, particularly ruthenium, Raney catalysts which can hydrogenate (1) aromaticity-exhibiting ring portions of organic compounds, (2) carboxylic acids and their ester portions (carbonyl ester groups), (3) ring portions and carboxylic acid or their ester groups in compounds having such ring portions and carboxylic acid or their ester portions, and (4) ring portions and nitrile groups of aromatic nitrile compounds and methods for the preparation of corresponding hydrogenated compounds. The methods allow preparation of hydrogenated compounds having hydrogenated aromatic ring portions, hydrogenated carbonyl ester groups, hydrogenated aromatic ring and carbonyl ester groups, or hydrogenated aromatic rings and nitrile groups under milder hydrogen pressure and temperature conditions than the conventional catalysts.

Metal raney catalysts and preparation of hydrogenated compounds therewith

Noble metal raney catalysts and preparation of hydrogenated compounds therewith

Noble metal, particularly ruthenium, Raney catalysts having the property of catalyzing the hydrogenation of (1) aromaticity-exhibiting ring portions of organic compounds, (2) carboxylic acids and their ester portions (carbonyl ester groups), (3) ring portions and carboxylic acid or their ester groups in compounds having such ring portions and carboxylic acid or their ester portions, and (4) ring portions and nitrile groups of aromatic nitrile compounds and methods for the preparation of corresponding hydrogenated compounds. The methods allow preparation of hydrogenated compounds having hydrogenated aromatic ring portions, hydrogenated carbonyl ester groups, hydrogenated aromatic ring and carbonyl ester groups, or hydrogenated aromatic rings and nitrile groups under milder hydrogen pressure and temperature conditions than the conventional catalysts.

Noble metal Raney catalysts and preparation of hydrogenated compounds

A process for the hydroformylation of allyl alcohol is disclosed, which comprises reacting allyl alcohol with carbon monoxide and hydrogen in the presence of a rhodium compound and a diphosphine compound represented by formula (I) or (II) ##STR1## wherein R.sup.1 represents an alkyl group or a substituted or unsubstituted aryl group; and R.sup.2 and R.sup.3 each represents an alkyl group or a hydrogen atom.

Hydroformylation of allyl alcohol

The subject invention relates to an ointment comprising a homogeneous mixture of polymer or copolymer of N-vinylacetamide, as an essential component, water and/or alcohols, and a pharmacologically active component. The ointment may be coated or plastered onto the skin or mucosa of a human being or animal in order to effect a therapeutic response.

Ointment comprising a homogenous mixture of a polymer or copolymer of

A (co)polymer suitable for bases or auxiliary agents for external application (for example, hydrophilic gels, adhesives, thickeners or excipients) to be coated or plastered onto the skin or mucosa of a human being or animal, such as ointment agents (ointment, hydrogel, jelly or cream), plastering agents (molded poultice, tape agent or plaster agent), sticky bandages (sticky bandage, strap, wound strap, surgical tape, taping material, supporter), and to preparations for external application containing same.

External application base or auxiliary agent and external application

An allyl ester oligomer composition having a viscosity of 200 to 50,000 cP at 30.degree. C. and a refractive index of 1.50 to 1.57 at 30.degree. C., which is formed by mixing (a) 20 to 90% by weight of an allyl ester oligomer, (b) 10 to 80% by weight of at least one polyvalent allyl ester monomer selected from the group consisting of diallyl phthalate, diallyl isophthalate, diallyl terephthalate, diallyl adipate, triallyl (iso)cyanurate and triallyl trimellitate, and (c) up to 40% by weight of at least one monofunctional polymerizable monomer selected from the group consisting of vinyl benzoate, allyl benzoate, phenyl (meth)acrylate and benzyl (meth)acrylate.

Allyl ester oligomer composition and organic glass for optical material

A diallyl terephthalate prepolymer consisting essentially of diallyl terephthalate monomer units, having

Diallyl terephthalate prepolymer and process for producing seam

A process for the preparation of an N-(.alpha.-alkoxyethyl)carboxylic acid amide represented by the following formula [I]: ##STR1## wherein R stands for a hydrogen atom, an alkyl group having 1 to 6 carbon atoms, a benzyl group or an aryl group, and R.sup.1 stands for an alkyl group having 1 to 10 carbon atoms or a cycloalkyl group, which comprises reacting an ethylidene-bisamide represented by the following formula [II]:

Process for preparation of N-(.alpha.-alkoxyethyl)-carboxylic acid amide

A diallyl terephthalate prepolymer is here disclosed which essentially has the following structure

Novel diallyl terephthalate prepolymer and method for preparing it

A monoalkylene glycol monoether is produced with good efficiency and commercial advantage by reacting an alkylene oxide with an alcohol in the presence of a solid catalyst resulting from the exchange of exchangeable cations of a montmorillonite clay with a cation of Al, Cr, Mn, Fe, Sn or Th.

Process for preparing monoalkylene glycol monoethers

Ethyl acetate and an excess of ethylene glycol monoethyl ether are subjected to ester-interchange reaction at a temperature not exceeding 100.degree. C. in the presence of a strongly acidic cation exchange resin as a catalyst. The resulting reaction mixture is distilled to recover the ethylene glycol monoethyl ether acetate formed. The unchanged reactants are recycled to the reaction zone for re-use, and the by-product ethanol is recovered in a highly pure form. This method can be continuously performed easily and effectively without the need to separate the catalyst or to employ complex distilling steps and without involving other difficulties.

Process for the continuous production of ethylene glycol monoethyl ether

A process for preparing 3-cyanopyridine by the ammoxidation of 2-methyl-5-ethylpyridine which comprises reacting 2-methyl-5-ethylpyridine with ammonia and oxygen in the vapor phase at an elevated temperature, using a specific catalyst consisting of a low-area carrier on which has been deposited vanadium oxide and other specific metal oxides, the reaction being carried out in the copresence of steam.

Growing community of inventors

Oita, Japan

Kuniomi Marumo