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公开(公告)号:JPH04235976A
公开(公告)日:1992-08-25
申请号:JP7354791
申请日:1991-01-18
Applicant: UBE INDUSTRIES
Inventor: FUJII KATSUTOSHI , FUKUDA YASUHISA , YAMANAKA YOSHINORI
IPC: A01N43/54 , C07D239/42 , C07D239/47 , C07D239/48 , C07D239/70 , C07D239/94 , C07D239/95 , C07D513/04
Abstract: PURPOSE:To profitably produce an aralkylaminopyrimidine compound useful as an antimicrobial agent by reacting a pyrimidine compound with an aralkylamine compound in an alcoholic solvent. CONSTITUTION:A compound of formula I (R is halogen, alkyl, H; R is alkyl, halogen, or R and R may be condensed with the pyrimidine ring with the carbon atoms bonded to the R and R , respectively, to form a saturated or unsaturated five or six-membered ring which may contain a sulfur atom; R is H, alkyl, etc.; X is a releasable group) is reacted with a compound of formula II (R is alkyl, haloalkyl, H, etc.; R is halogen, H; R is H, alkyl, halogen, etc.; n is 1,2) preferably in a ratio of 1:0.5-1.5 in the presence of a base in an alcoholic solvent such as methanol preferably at 70-14 deg.C for 1-4hr, followed b by purifying the solution product by various chromatographic methods to provide the objective compound of formula III.
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公开(公告)号:JPH04164072A
公开(公告)日:1992-06-09
申请号:JP28725990
申请日:1990-10-26
Applicant: UBE INDUSTRIES
Inventor: OBATA TOKIO , FUJII KATSUTOSHI , FUKUDA YASUHISA , TSUTSUMIUCHI KIYOSHI
IPC: C07D239/34 , A01N43/54 , C07D239/70 , C07D495/04
Abstract: NEW MATERIAL:A compound of formula I (R is 1-4C alkyl or halogen; R is 1-4C alkyl; R and R is, together with C, condensed with pyrimidine ring into a five-membered ring; A is -CH2CH2- or -CH(CH3)-). EXAMPLE:dl-5-Chloro-6-ethyl-[1-(4-tert-butylphenyl)ethoxy] pyrimidine. USE:A pest control agent. Having excellent control effects on Hemiptera, Lepidoptera, Coleoptera, mite, sanitary insect pests, stored grain insect pests, etc. Also having control effects on agricultural/horticultural pathogenic bacteria such as for wheat brown rust, downy mildew, and neck rot. PREPARATION:The objective compound of the formula I can be obtained by reaction between a compound of formula II (X is eliminable group) and another compound of formula III pref. in a solvent (e.g. DMF) in the presence of a base (e.g. NaH) at room temperature to the boiling point.
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公开(公告)号:JPH03223257A
公开(公告)日:1991-10-02
申请号:JP8060290
申请日:1990-03-30
Applicant: UBE INDUSTRIES
Inventor: OBATA TOKIO , FUJII KATSUTOSHI , FUKUDA YASUHISA , TSUTSUMIUCHI KIYOSHI
IPC: C07D231/20 , A01N43/56
Abstract: NEW MATERIAL:A pyrazole oxime derivative expressed by formula I (R1 is H, halogen or 1-5C alkyl; R2 is H or 1-5C alkyl; R3 is 1-8C alkyl, 3-5C alkenyl, 3-5C alkynyl or aralkyl which may be substituted; R4 is H or 1-5C alkyl; (n) is 1-3; A is 1-5C alkylene; X is O or S). EXAMPLE:[1,3-Dimethyl-5-phenoxypyrazole-4-formaldoxime 0-2-[4-(2- methoxyethyl)phenoxy]ethyl ether. USE:Useful as an insecticide, acaricide and germicide. PREPARATION:A compound expressed by formula II is subjected to a reaction with a compound expressed by formula III (Y is eliminable group) in a solvent in the presence of a base or a compound expressed by formula II and a compound expressed by formula III are heated and dissolved to provide the compound expressed by formula I.
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公开(公告)号:JPH0142257B2
公开(公告)日:1989-09-11
申请号:JP13802382
申请日:1982-08-10
Applicant: UBE INDUSTRIES
Inventor: TAKEMATSU TETSUO , TAKEUCHI YASUTOMO , TAKENAKA MASAAKI , TAKAMURA SEIJI , NISHIMURA MINORU , OKADA TATSUO , FUKUDA YASUHISA
IPC: C07D317/58 , A01N39/02 , A01N43/06 , A01N43/08 , A01N43/30 , A01N43/40 , C07C67/00 , C07C231/00 , C07C235/20 , C07C239/14 , C07D213/40 , C07D307/52 , C07D333/20
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公开(公告)号:JPS58113155A
公开(公告)日:1983-07-05
申请号:JP20994581
申请日:1981-12-28
Applicant: UBE INDUSTRIES
Inventor: TAKEMATSU TETSUO , TAKEUCHI YASUTOMO , TAKENAKA MASAAKI , TAKAMURA SEIJI , NISHIMURA MINORU , OKADA TATSUO , FUKUDA YASUHISA
IPC: C07D333/24 , A01N39/02 , A01N39/04 , A01N43/06 , A01N43/08 , A01N43/40 , C07C67/00 , C07C231/00 , C07C235/06 , C07C235/20 , C07D213/40 , C07D307/52 , C07D333/20
Abstract: NEW MATERIAL:Phenoxyalkanoic acid amide derivative of formulaI(X is lower alkyl, halogen, nitro; n is 0-3; R is lower alkyl; Y is furyl, thienyl, pyridyl, naphthyl). EXAMPLE:N-Thienylmethyl-2-(4-chloro-3,5-dimethylphenoxy)-butylamide. USE:Herbicide: it has herbicidal effect against bloadleaf weeds and other kinds of weeds by whitening and hardly exerts injury to gramineous crops and other ones. Further, it has no toxicity to men, animals, fish and shells and no strange odor. PREPARATION:The reaction of a compound of formula II (Z is Cl, Br) with another compound of formula III is conducted in a solvent such as benzene, methyl ethyl ketone, by adding a weak alkali such as pyridine, at 0-30 deg.C to give the compound of formulaI.
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公开(公告)号:JP2015179792A
公开(公告)日:2015-10-08
申请号:JP2014057410
申请日:2014-03-20
Applicant: UBE INDUSTRIES
Inventor: ENDO KENTA , HIROTSU KENJI , FUKUDA YASUHISA
IPC: H01G9/035
Abstract: 【課題】本発明は、電解質化合物の析出がなく、安定に使用することができる、高耐電圧の電解コンデンサ電解液の提供を課題とする。【解決手段】本発明の課題は、特定のN−アシルグルタミン酸又はその塩を電解質として用いた電解コンデンサ用電解液及び電解コンデンサにより解決される。さらに本発明のN−アシルグルタミン酸又はその塩を含有した電解コンデンサ用電解液を用いた電解コンデンサは、低温溶解性、耐電圧性に優れており、電解コンデンサ用電解液の電解質として好適に使用することができる。【選択図】なし
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37.
公开(公告)号:JP2003146959A
公开(公告)日:2003-05-21
申请号:JP2001349725
申请日:2001-11-15
Applicant: UBE INDUSTRIES
Inventor: NISHINO SHIGEYOSHI , FUKUDA YASUHISA , MURAKAMI TADASHI , OGAMI MASAYOSHI , YAMADA SHUJI
IPC: C07C251/76 , C07C249/16 , C07C253/30 , C07C255/66
Abstract: PROBLEM TO BE SOLVED: To provide a new 3-halo-2-hydrazono-1-hydroxyiminopropane derivative useful as medical and agrochemical intermediates and to provide a method for producing the derivative. SOLUTION: A 3-halo-2-oxo-1-hydroxyiminopropane derivative represented by formula (2) [R is COOR (wherein R is a lower alkyl group or a cycloalkyl group) or cyano group; X is a halogen atom] is reacted with a hydrazine derivative represented by formula (3) H2 NNHR [wherein R is a lower acyl group] to produce the 3-halo-2-hydrazono-1-hydroxyiminopropane derivative represented by formula (1) [wherein R , R and X are each as described above].
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公开(公告)号:JP2002114748A
公开(公告)日:2002-04-16
申请号:JP2000303402
申请日:2000-10-03
Applicant: UBE INDUSTRIES
Inventor: HARADA KATSUMASA , FUKUDA YASUHISA , YAMANAKA YOSHINORI , MURAKAMI TADASHI
IPC: C07C253/00 , C07C255/24
Abstract: PROBLEM TO BE SOLVED: To provide 12-amino-4,8-dodecadienenitrile as an intermediate material for 12-aminododecanoic acid or the like, and to provide a method for producing the nitrile. SOLUTION: This method for producing 12-amino-4,8-dodecadienenitrile as a new compound is characterized by comprising, for example, reducing 2- aminocyclododecadienone oxime with a reducing agent.
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公开(公告)号:JP2002088041A
公开(公告)日:2002-03-27
申请号:JP2000274723
申请日:2000-09-11
Applicant: UBE INDUSTRIES
Inventor: HARADA KATSUMASA , FUKUDA YASUHISA , YAMANAKA YOSHINORI , MURAKAMI TADASHI , HIROTSU KENJI
IPC: C07C253/00 , C07C255/04 , C07C255/09
Abstract: PROBLEM TO BE SOLVED: To provide a new method for production aiming at improving the yield of an α,ω-dicyano compound and simplifying the process. SOLUTION: This method for producing the α,ω-dicyano compound is characterized by reacting 2-alkoxycycloalkanone oximes with formic acid and hydroxylamine.
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公开(公告)号:JPH11240874A
公开(公告)日:1999-09-07
申请号:JP4151698
申请日:1998-02-24
Applicant: UBE INDUSTRIES
Inventor: TAKAHASHI KAZUFUMI , TANAKA TOSHIFUSA , FUKUDA YASUHISA , KUWATA TAKAAKI , NORITAKE TOMOYA
IPC: C07D271/08 , A01N43/832 , C07D413/06
Abstract: PROBLEM TO BE SOLVED: To obtain the subject germicide having an excellent germicidal effect and exerting controlling effect on cucumber mildew, rice blast disease or the like by using a specified dicarbonylfuroxan compound as an active ingredient. SOLUTION: This germicide contains a clicarbonylfuroxan compound of the formula (R and R are each phenyl, a 1-12C alkyl or the like) as an active ingredient. Among the compounds of the formula, bis(3,4-dimethoxybenzoyl) furoxan, bis(3,4-methylenedioxybenzoyl)furoxan, bis(4-difluoromethoxybenzoyl) furoxan, bis(3-thenoyl)furoxan, bis(heptanoyl)furoxan and bis(decanoyl)furoxan are each a new compound. The compound of the formula is obtained from the corresponding methyl ketone body. The active ingredient concentrations in the form of preparations are preferably 1-50 wt.%, 0.3-25 wt.%, 0.5-10 wt.%, 0.5-5 wt.% and 0.1-5 wt.% for an emulsion, powder, granules, oil and aerosol, respectively.
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