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公开(公告)号:DE68915073T2
公开(公告)日:1994-08-18
申请号:DE68915073
申请日:1989-02-07
Applicant: DAICEL CHEM
Inventor: YOKOTA SHIGERU , TANAKA YASUTAKA , MIYAKE HIROTO
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公开(公告)号:DE3850647D1
公开(公告)日:1994-08-18
申请号:DE3850647
申请日:1988-01-13
Applicant: DAICEL CHEM
Inventor: YAGII TOYOKAZU , ITOKAZU TERUO , OKA KENJI , TANAKA YASUTAKA , KOJIMA HIDETAKA
IPC: C07C68/00 , C07C263/04 , C07C265/04 , C07C265/10 , C07C265/14 , C07C263/00
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公开(公告)号:DE68915073D1
公开(公告)日:1994-06-09
申请号:DE68915073
申请日:1989-02-07
Applicant: DAICEL CHEM
Inventor: YOKOTA SHIGERU , TANAKA YASUTAKA , MIYAKE HIROTO
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公开(公告)号:EP0987261A4
公开(公告)日:2003-02-05
申请号:EP99905217
申请日:1999-02-17
Applicant: DAICEL CHEM
Inventor: TANAKA YASUTAKA , UENAKAI HIROAKI , SHIMADA GIICHI
IPC: C07D317/26 , C07D317/22
CPC classification number: C07D317/26
Abstract: A process for producing a dialdehyde monoacetal (III) from a dialdehyde (I) and a diol (II), characterized by reacting the dialdehyde (I) with twice or more, on the molar basis, as much the diol (III) to give a dialdehyde bisacetal (IV) and then reacting this dialdehyde bisacetal (IV) with a dialdehyde (III); and a process for producing glutaraldehyde monoacetal by reacting 2-Y-3,4-dihydro-2H-pyran with a diol, characterized by reacting in the second step glutaraldehyde (iv) formed as a by-product with glutaraldehyde bisacetal (v) formed as another by-product to give glutaraldehyde monoacetal (iii).
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公开(公告)号:EP0354970A4
公开(公告)日:1990-06-26
申请号:EP89902082
申请日:1989-02-07
Applicant: DAICEL CHEM
Inventor: YOKOTA SHIGERU , TANAKA YASUTAKA , MIYAKE HIROTO
CPC classification number: C07C68/005 , C07C69/96
Abstract: A carbonic acid ester is produced by reacting an alcohol with both carbon monoxide and oxygen in the presence of a catalyst comprising a divalent copper atom in the form of a weak acid salt and/or halide and an alkaline earth metal in the form of a weak acid salt and/or halide.
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公开(公告)号:DE69612529D1
公开(公告)日:2001-05-23
申请号:DE69612529
申请日:1996-06-18
Applicant: DAICEL CHEM
Inventor: SAITOH MORIHITO , TANAKA YASUTAKA
IPC: B01J29/40 , B01J29/48 , C07D213/08 , C07D213/09 , C07D213/10 , B01J29/06 , C07D213/12
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公开(公告)号:DE3850647T2
公开(公告)日:1994-11-17
申请号:DE3850647
申请日:1988-01-13
Applicant: DAICEL CHEM
Inventor: YAGII TOYOKAZU , ITOKAZU TERUO , OKA KENJI , TANAKA YASUTAKA , KOJIMA HIDETAKA
IPC: C07C68/00 , C07C263/04 , C07C265/04 , C07C265/10 , C07C265/14 , C07C263/00
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公开(公告)号:GB2199030B
公开(公告)日:1990-09-05
申请号:GB8723895
申请日:1987-10-12
Applicant: DAICEL CHEM
Inventor: TANAKA YASUTAKA , KOJIMA HIDETAKA , TSUJI YASUO
Abstract: A process for preparing an alpha -phenylpropionic acid derivative wherein an alpha -phenylethyl alcohol derivative is reacted with carbon monoxide in the presence of a catalyst to give an alpha -phenylpropionic acid derivative, which comprises carrying out the reaction in either one of the following manners (I), (II) and (III): (i) effecting said reaction in the presence of a rhodium catalyst, as said catalyst, together with an iodine compound in such an amount as to give a Rh to I ratio on an atomic basis of 1:0.5 to 1:6; adjusting the concentration of water in the reaction mixture to a level of 2 mol/l or below; and employing a reaction temperature of 130 DEG C. or below, (II) employing a mixture of a hydrocarbon and an oxygen-containing organic compound as a solvent, or (III) effecting said reaction in the presence of a rhodium catalyst, as said catalyst, and an iodine compound; adding water optionally together with an oxygen-containing organic compound as an extraction solvent to the resulting reaction mixture to thereby separate the same into two layers, i.e., a layer containing the reaction product and an aqueous layer; and repeatedly using the rhodium catalyst contained in said aqueous layer.
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公开(公告)号:GB2199030A
公开(公告)日:1988-06-29
申请号:GB8723895
申请日:1987-10-12
Applicant: DAICEL CHEM
Inventor: TANAKA YASUTAKA , KOJIMA HIDETAKA , TSUJI YASUO
Abstract: A process for preparing an alpha -phenylpropionic acid derivative wherein an alpha -phenylethyl alcohol derivative is reacted with carbon monoxide in the presence of a catalyst to give an alpha -phenylpropionic acid derivative, which comprises carrying out the reaction in either one of the following manners (I), (II) and (III): (i) effecting said reaction in the presence of a rhodium catalyst, as said catalyst, together with an iodine compound in such an amount as to give a Rh to I ratio on an atomic basis of 1:0.5 to 1:6; adjusting the concentration of water in the reaction mixture to a level of 2 mol/l or below; and employing a reaction temperature of 130 DEG C. or below, (II) employing a mixture of a hydrocarbon and an oxygen-containing organic compound as a solvent, or (III) effecting said reaction in the presence of a rhodium catalyst, as said catalyst, and an iodine compound; adding water optionally together with an oxygen-containing organic compound as an extraction solvent to the resulting reaction mixture to thereby separate the same into two layers, i.e., a layer containing the reaction product and an aqueous layer; and repeatedly using the rhodium catalyst contained in said aqueous layer.
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公开(公告)号:JP2002322103A
公开(公告)日:2002-11-08
申请号:JP2001132080
申请日:2001-04-27
Applicant: DAICEL CHEM
Inventor: NISHIYAMA SATORU , TANAKA YASUTAKA
Abstract: PROBLEM TO BE SOLVED: To obtain the corresponding unsaturated cyclic alcohols at a high conversion rate and with a high selectivity from unsaturated cyclic aldehydes possessing unsaturated bonds within a cyclic group. SOLUTION: In the presence of a catalyst containing at least one species of metals selected from the group III, IV, IX, XIII and XIV of the periodic table and a secondary alcohol the corresponding unsaturated cyclic alcohol compound is prepared by reducing selectively the formyl group of the unsaturated cyclic aldehydes without reducing the unsaturated carbon - carbon bonds. As the unsaturated cyclic aldehydes, C5-16 mono- or tri-cyclo-alkenecarbaldehyde and the like can be employed. The reduction reaction may be carried out at 40-120 deg.C and under the hydrogen gas pressure of roughly 0.01-5 MPa.
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