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公开(公告)号:JPS6250459B2
公开(公告)日:1987-10-24
申请号:JP7373980
申请日:1980-06-03
Applicant: MITSUI TOATSU CHEMICALS
Inventor: TAKAGI USAJI , KASUGA TAKAHARU , TSUMURA RYUICHIRO
IPC: B01J31/00 , B01J31/02 , C07C67/00 , C07C201/00 , C07C201/10 , C07C205/02
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公开(公告)号:JPS6160826B2
公开(公告)日:1986-12-23
申请号:JP14448479
申请日:1979-11-09
Applicant: MITSUI TOATSU CHEMICALS
Inventor: TSUMURA RYUICHIRO , TAKAGI USAJI , KASUGA TAKAHARU , IKEDA KEIICHI
IPC: C07B61/00 , B01J31/00 , B01J31/02 , B01J31/18 , C07C67/00 , C07C241/00 , C07C265/00
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公开(公告)号:JPS577456A
公开(公告)日:1982-01-14
申请号:JP8018080
申请日:1980-06-16
Applicant: MITSUI TOATSU CHEMICALS
Inventor: TSUMURA RIYUUICHIROU , TAKAGI USAJI , KASUGA TAKAHARU , IKEDA KEIICHI
Abstract: PURPOSE:The reaction between an aromatic nitro compound and carbon monoxide is conducted in the presence of a maine catalyst of a noble metal and a cocatalyst of a compound of a metal of VA group at high temperature under high pressure to produce the titled compound used as a raw material of polyurethane directly in high yield. CONSTITUTION:At least one selected from a mixture of a compound of noble metal such as Ru and a heteroaromatic nitrogen compound such a pyrrole, a complex of noble metal coordinated by the above nitrogen compound such as bis(pyridine) dichloropalladium (II) and a mixture of the complex and the nitrogen compound is used as a main catalyst and at least one of cyclopentadienyl halide of transition metal of group VA in the periodic table is used as a cocatalyst to effect the reaction between an aromatic nitro compound such as nitrobenzene and carbon monoxide at high temperature under high pressure, thus producing the titled compound. The addition of the cocatalyst permits the reduction in the main catalyst required to about 1/10 of the amount used in the conventional process and facilitates are recovery.
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公开(公告)号:JPH09169727A
公开(公告)日:1997-06-30
申请号:JP33352895
申请日:1995-12-21
Applicant: MITSUI TOATSU CHEMICALS
Inventor: KASUGA TAKAHARU , HARA RETSU , TAKAGI USAJI
IPC: C07D209/08 , B01J23/28 , B01J31/02 , C07B61/00
Abstract: PROBLEM TO BE SOLVED: To efficiently obtain indole or indole analogues from inexpensive raw materials through one-step reaction using a new catalyst. SOLUTION: An aniline analogue, for example, aniline and a 1,2-glycol, for example, ethylene glycol are allowed to react with each other in a liquid phase in the presence of a molybdic acid or a molybdenum oxide.
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公开(公告)号:JPH08164336A
公开(公告)日:1996-06-25
申请号:JP30762394
申请日:1994-12-12
Applicant: MITSUI TOATSU CHEMICALS
Inventor: KASUGA TAKAHARU , TAKAMURA KAZUO , HARA RETSU , TAKAGI USAJI
IPC: C07D209/08 , B01J23/78 , C07B61/00
Abstract: PURPOSE: To efficiently produce indole or indole derivatives from an inexpensive raw material with one stage of liquid phase reaction. CONSTITUTION: A complex oxide catalyst containing Si, Cu and Mg for production of indole or indole derivatives is prepared by adding a basic aqueous liquid of a Si compound to an aqueous liquid containing a Cu compound and a Mg compound to produce coprecipitation.
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公开(公告)号:JP2505456B2
公开(公告)日:1996-06-12
申请号:JP10328787
申请日:1987-04-28
Applicant: MITSUI TOATSU CHEMICALS
Inventor: ONO HIROSHI , KASUGA TAKAHARU , HEN PARAA , KYONO SHINJI
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公开(公告)号:JPH0871420A
公开(公告)日:1996-03-19
申请号:JP21290294
申请日:1994-09-06
Applicant: MITSUI TOATSU CHEMICALS
Inventor: KASUGA TAKAHARU , TAKAMURA KAZUO , HARA RETSU , TAKAGI USAJI
IPC: C07D209/08 , B01J23/72 , C07B61/00
Abstract: PURPOSE: To obtain a catalyst for industrially producing indole or its derivatives by using inexpensive starting materials and a single-stage liquid phase reaction by adding a base to a homogeneous aq. solution contg. a silicate, a copper compound, a magnesium compound and a mineral acid.to effect coprecipitation. CONSTITUTION: This catalyst for producing indole or its derivatives from one of anilines and one of 1,2-glycols is obtained by preparing a homogeneous aq. solution contg. a silicate a copper compound, a magnesium compound and a mineral acid and thereafter, adding a base to the solution to effect coprecipitation. For example, a copper compound.and a magnesium compound are added to a mineral acid--acidic solution of a water-soluble silicate to form a homogeneous aq. solution and then, a base is added to the resulting aq. solution to obtain coprecipitated solid hydroxide and thereafter, the solid hydroxide is dried and calcined. Preferably, the pH of the homogeneous aq. solution before adding the base is
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公开(公告)号:JPH0611743B2
公开(公告)日:1994-02-16
申请号:JP3055285
申请日:1985-02-20
Applicant: MITSUI TOATSU CHEMICALS
Inventor: TSUMURA RYUICHIRO , MYATA KATSUJI , KASUGA TAKAHARU , IKEDA KEIICHI
IPC: C07B61/00 , B01J31/00 , B01J31/02 , B01J31/22 , B01J31/36 , C07C67/00 , C07C241/00 , C07C263/14 , C07C265/00 , C07C265/12 , C07C265/14
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公开(公告)号:JPH06713B2
公开(公告)日:1994-01-05
申请号:JP23641285
申请日:1985-10-24
Applicant: MITSUI TOATSU CHEMICALS
Inventor: ONO HIROSHI , KASUGA TAKAHARU
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公开(公告)号:JPS6416745A
公开(公告)日:1989-01-20
申请号:JP17286587
申请日:1987-07-13
Applicant: MITSUI TOATSU CHEMICALS
Inventor: ONO HIROSHI , KASUGA TAKAHARU , KIYONO SHINJI
Abstract: PURPOSE:To obtain the titled compound having uses of wide range such as an intermediate for synthesizing industrial chemicals and capable of readily controlling also oxidation rate without by-product in advantageous conditions, by oxidizing 2-chloropropionic aldehyde with oxygen, etc., in the presence of a specific metal compound catalyst in a liquid phase. CONSTITUTION:2-Chloropropionic aldehyde which is a raw material is oxidized in the presence of at least one kind of metal compound catalyst selected from a palladium compound or platinum compound as a catalyst in a liquid phase with oxygen or an oxygen-containing gas at 20-120 deg.C, preferably 40-80 deg.C to provide the aimed compound. The above-mentioned reaction is preferably carried out using a solvent such as acetic acid and in a concentration of raw material in the solvent in the range of normally 1-50wt.%, especially 5-15wt.%. Further more, as the above-mentioned catalyst, e.g. palladium black, palladium oxide, platinum black, platinum dioxide is preferably used in a liquid phase in the range of 0.01-5wt.%.
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