Mitsui Toatsu Chemicals, Incorporated

Mitsui Chemicals, Inc.

Tamotsu Asano

Tsutomu Ishii

Naoki Sato

Hideo Yamazaki

Masatoshi Gohbara

Mitsumasa Umemoto

Junko Watanabe

Kiyoshi Ito

Makoto Nishida

Shuji Ozawa

Seiichi Watanabe

Takeya Abe

Kenju Sasaki

Teruyuki Nagata

Masao Imai

Nobuhiro Fukuda

Nobuyuki Fukazawa

Tomoyuki Ando

Satoshi Numata

Tadashi Araki

Takeshi Nakamura

Hitoshi Shimotori

Hironori Komatsu

Katsutoshi Tsuchiya

Takeshi Nishida

Kanemitsu Miyama

Hiroki Ishibashi

Yasushi Fukuiri

Toshio Matsumoto

Kiyoshi Itou

Hitoki Miyake

Hideki Umetani

Akinobu Takagi

Ichirou Ikeda

Shohei Nozaki

Takeshi Imakita

Hironobu Horie

Seiichi Shimono

Junya Fujiwara

Nobuyasu Tamura

Yoshinobu Shimura

Takahiro Yamauchi

Yukio Kiritani

Yuuji Enomoto

Masaru Arai

Satoru Iwamori

Toshihisa Tachibana

Kyoko Maruyama

Hirokazu Awano

Katsuyuki Takahashi

The invention is to provide a process for effectively removing impurities contained in an amide compound-containing solution by making an amide compound-containing solution, particularly an amide compound-containing solution produced by a hydration reaction of a nitrile compound by using a microorganism fungus body containing nitrile hydratase or a processed product of the microorganism fungus body, in contact with activated carbon under acidic conditions.

Method of purifying amide compound

A desired isomer is selectively prepared by phosphorolyzing and isomerizing an anomer mixture of a 1-phosphorylated saccharide derivative while crystallizing one of the isomers to displace the equilibrium. Furthermore, using the action of a nucleoside phosphorylase, a nucleoside is prepared from the 1-phosphorylated saccharide derivative obtained and a base with improved stereoselectivity and a higher yield. This process is an anomer-selective process for preparing a 1-phosphorylated saccharide derivative and a nucleoside.

Process for selectively producing 1-phosphorylated sugar derivative anomer and process for producing nucleoside

The invention is a process for continuously producing an amide compound by reacting a microorganism fungus body containing nitrile hydratase or a processed product of the microorganism fungus body with a nitrile compound in an aqueous medium, characterized in that after contacting said fungus body or said processed product of said fungus body with said nitrile compound in said aqueous medium, a reaction solution thus obtained is further subjected to reaction under conditions having a plug flow region, and according to the invention, an amide compound aqueous solution of a high concentration a high purity can be easily obtained in an extremely high conversion rate of a nitrile compound without a condensation process.

Process for producing amide compounds

Described are a stick-shaped soil fumigant preparation and an application method therefor. The fumigant preparation comprises a water-soluble and/or biodegradable film and a soil sterilizer and/or nematocide hermetically packed in the form of a stick with the film. The soil sterilizer and nematocide are each in a liquid form at room temperature. The soil fumigant preparation according to the present invention remains suppressed in toxicity, volatility and irritation before application to the soil, but its active ingredient(s) are promptly released after application. In addition, the present invention makes it possible to provide a fumigant in such a form as permitting a substantial improvement in the efficiency of work by a fumigating worker and also to provide an effective application method therefor, without the need for any machine designed exclusively for fumigation.

Soil fumigant preparations

An aqueous suspension-type microcapsule insecticide composition which is obtained by emulsifying a hydrophobic admixture of liquid pyrethroid insecticide or a pyrethroid insecticide and a high boiling point solvent, preferably an alkyl ester of phthalic acid in which the alkyl group has 8-13 carbon atoms to form particles of a suitable size in the presence of an anionic water-soluble polymeric surface active agent and polycondensating melamine-formaldehyde or a derivative thereof on the surface of the said emulsified and dispersed particles, and a process for producing the composition. This composition exhibits stable insecticidal activity over a prolonged period with noticeably reduced toxicity to aquatic life.

Insecticide composition and production process thereof

Disclosed are herbicidally active pyrimidine derivatives of the formula ##STR1## wherein R represents a hydrogen atom or an etherifying group, e.g., a lower alkyl, lower alkenyl, lower alkynyl, phenyl-substituted lower alkenyl, lower haloalkenyl, cycloalkyl, substituted phenyl-substituted lower alkenyl or phenyl-substituted lower alkynyl group; or a group represented by the following formula: ##STR2## wherein R.sup.1 represents a hydrogen atom or a lower alkyl group, X a halogen atom or a lower alkyl or lower alkoxyl group, m and n individually 0-2, and when m is 2, both Xs may be the same or different, and herbicidal compositions containing the same, alone or in combination with another herbicidally active compound, the pyrimidine derivatives being prepared by reaction of 2-(4,6-dimethoxy-2-pyrimidinyloxy)benzaldehyde with NH.sub.2 OR or with a salt of hydroxylamine followed by reaction with a halide of the formula RY wherein R has the same value as above and Y is Cl, Br or I.

Pyrimidine derivatives, preparation processes thereof, herbicide

2-(4,6-dimethoxy-2-pyrimidinyloxy)benzaldoximes, preparation processes

Process for preparation of 3-phenoxybenzyl

The present invention relates to a process for producing 3-phenoxybenzyl 2-(4-alkoxyphenyl)-2-methylpropyl ethers having excellent insecticidal and acaricidal activities which are represented by formula (IV): ##STR1## wherein R is a lower alkyl group and X.sub.1 and X.sub.2 are each a hydrogen or fluorine atom, which comprises reacting a 3-halogeno-4-alkoxyneophyl halide represented by the formula (I): ##STR2## wherein Y.sub.1 and Y.sub.2 are each a hydrogen, chlorine or bromine atom, at least one of them being a chlorine or bromine atom, R has the same meaning as above and X is a halogen atom, with a 3-phenoxybenzyl alcohol represented by the formula (II): ##STR3## wherein X.sub.1 and X.sub.2 have the same meaning as above, in the presence of a base to obtain a 3-phenoxybenzyl 2-(4-alkoxy-3-halogenophenyl)-2-methylpropyl ether represented by the formula (III): ##STR4## wherein Y.sub.1, Y.sub.2, R, X.sub.1 and X.sub.2 have the same meaning as above, and then subjecting the product to a hydrodehalogenation reaction, and relates to a process for producing a 3-halogeno-4-alkoxyneophyl halide represented by formula (I), which comprises reacting a 2-halogeno-1-alkoxybenzene represented by formula (V): ##STR5## wherein Y.sub.1 and Y.sub.2 are each a hydrogen, chlorine or bromine atom, at least one of them being a chlorine or bromine atom, and R represents a lower alkyl group, with a methallyl halide in the presence of an acid catalyst at -20.degree. to 50.degree. C.

Process for producing 3-phenoxybenzyl 2-(4-alkoxyphenyl)-2-methylpropyl

Growing community of inventors

Chiba, Japan

Tamotsu Asano