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公开(公告)号:JPH10130237A
公开(公告)日:1998-05-19
申请号:JP29544197
申请日:1997-10-28
Applicant: BASF AG
Inventor: JULIUS MANFRED DR
IPC: C07D211/58 , C07D211/72
Abstract: PROBLEM TO BE SOLVED: To produce the subject compound in a high selectivity and good yield according to a new method for reacting 2,2,6,6-tetramethylpiperidine-4-one (TAA) with 4- amino-2,2,6,6-tetramethylpiperidine (TDA) through 2,2,6,6-tetramethyl-4-[(2,2,6,6- tetramethyl-4-piperidylidene) amino]-piperidine which is an intermediate while eliminating an impurity such as water requiring the separation for producing a light stabilizer. SOLUTION: 2,2,6,6-tetramethylpiperidine-4-one represented by formula I is reacted with 4-amino-2,2,6,6-tetramethylpiperidine represented by formula II to provide 2,2,6,6- tetramethyl-4-[[2,2,6,6-tetramethyl-4-piperidylidene] amino] piperidine represented by formula III, which is then reacted with NH3 and hydrogen in the presence of a hydrogenating catalyst to afford a compound represented by formula II. In order to obtain 2mol equiv. compound represented by formula II, the respective amounts of the compounds represented by formula I and II are 1mol equiv. and the reaction is carried out according to a reactional formula represented by formula IV. The compound represented by formula III is produced by carrying out the reaction in the absence of a catalyst at 30-90 deg.C and then aminating hydrogenation is directly conducted at 100 deg.C under 250 bars by using an excessive amount of NH3 to afford the compound represented by formula II.
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公开(公告)号:JPH10139744A
公开(公告)日:1998-05-26
申请号:JP29437297
申请日:1997-10-27
Applicant: BASF AG
Inventor: JULIUS MANFRED DR
IPC: C07C231/04 , C07C233/00 , C07D211/58
Abstract: PROBLEM TO BE SOLVED: To obtain an amide by reacting a specific diamine with a ketene to acetylate a sterically non-hindered amino functional group of the diamine. SOLUTION: This method for acetylating a diamine having a sterically hindered amino functional group (existing in a heterogeneous ring) and a sterically non-hindered amino functional group (e.g. 4-amino-2,2,6,6,- tetramethylpiperidine) comprises reacting the diamine with a ketene in an aprotic solvent (especially tetrahydrofuran) at -30 to 65 deg.C (preferably in the atmospheric pressure and/or by a batch type method. Thus, the objective compound (especially 4-acetamido-2,2,6,6-tetramethylpiperidine) is profitably obtained.
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公开(公告)号:JPH10130238A
公开(公告)日:1998-05-19
申请号:JP29419397
申请日:1997-10-27
Applicant: BASF AG
Inventor: JULIUS MANFRED DR
IPC: C07D211/02 , C07D211/58
Abstract: PROBLEM TO BE SOLVED: To produce the subject high-purity compound, useful as an intermediate important for producing various light stabilizers and hardly containing colored impurities according to an inexpensively practicable method without using an elaborate apparatus. SOLUTION: A compound represented by formula I is reacted with H2 in the presence of a hydrogenating catalyst to afford a compound represented formula II. The reaction is preferably carried out at a temperature within the range of 20-150 deg.C and the pressure is preferably within the range of 1-300bars. the hydrogenation of the compound represented by formula I for producing the compound represented by formula II is conducted in an autoclave by using a suspended catalyst, etc., according to a batch method or continuously carried out on a fixed bed catalyst in a cylindrical reactional furnace. the chemical reaction is carried out according to a chemical formula represented by formula III.
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4.
公开(公告)号:JPH10291976A
公开(公告)日:1998-11-04
申请号:JP5339098
申请日:1998-03-05
Applicant: BASF AG
Inventor: VOIT GUIDO DR , WITZEL TOM DR , JULIUS MANFRED DR
IPC: C07D211/12 , B01J21/04 , B01J21/06 , B01J21/08 , B01J31/02 , C07B61/00 , C07D211/58
Abstract: PROBLEM TO BE SOLVED: To obtain 4-amino-2,2,6,6-tetramethylpiperidine from 2,2,6,6- tetramethyl-4-piperidinone by an industrially excellent method in terms of cost by using a specific catalyst. SOLUTION: This 4-amino-2,2,6,6-tetramethylpiperidine of formula I is obtained by reacting 2,2,6,6-tetramethyl-4-piperidinone of formula II with ammonia in the presence of an acidic metal oxide catalyst or a solid acidic catalyst insoluble in a reaction mixture (except an ammonium-type inorganic and organic ion-exchanging substance) to obtain an imine substance of formula III, and subjecting to hydrogen addition in the presence of a hydrogenation catalyst. Preferably, aluminum oxide, silicon dioxide, bentonite, aluminum hydrosilicate of montmorillonite-type, aluminum silicate of erionite-type, etc., is used as the catalyst for obtaining the imine substance by the reaction.
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公开(公告)号:JPH10130239A
公开(公告)日:1998-05-19
申请号:JP22345797
申请日:1997-08-20
Applicant: BASF AG
Inventor: JULIUS MANFRED DR
IPC: C07D221/20 , B01J27/16 , C07B61/00 , C07D211/74
Abstract: PROBLEM TO BE SOLVED: To avoid the production of an O-acetylated enol and simply and economically produce the subject compound by reacting 4-piperidone with a ketene in the presence of an acidic catalyst. SOLUTION: An unacetylated 4-piperidone is reacted with a ketene in the presence of an acidic catalyst at 20-120 deg.C to provide a compound represented by the formula. The catalyst used is the one having
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公开(公告)号:JP2000143603A
公开(公告)日:2000-05-26
申请号:JP31254499
申请日:1999-11-02
Applicant: BASF AG
Inventor: JULIUS MANFRED DR , SCHNEIDER ROLF , MUNDINGER KLAUS DR , FISCHER JAKOB
IPC: B01J31/02 , C07B61/00 , C07C253/14 , C07C255/17 , C07C255/19
Abstract: PROBLEM TO BE SOLVED: To produce a cyanoacetic acid ester useful as an intermediate for producing an effective substance, an active substance such as caffeine, or a photoprotective substance advantageously on an industrial scale by reacting a corresponding monochloroacetic acid ester with hydrogen cyanide in the presence of a specific base. SOLUTION: A corresponding monochloroacetic acid ester is made to react with hydrogen cyanide in the presence of a basic compound (the amount of the base is commonly 50-300 mol.% based on the monochloroacetic acid ester) selected from a group consisting of tertiary amines (e.g. trialkylamine), salts of carbonic acid (e.g. an alkali metal carbonate), salts of a carbonic acid half ester) (e.g. an alkali metal alkylcarbonic acid salt), salts of a carboxylic acid (e.g. an alkali metal carboxylate), amidines (e.g. peralkylated amidine or a bicyclic amidine), guanidines (e.g. peralkylated guanidine) and aromatic N- heterocyclic compounds (e.g. pyridine) generally at -78 deg.C to 20 deg.C under 0.05-2 MPa for 10 min to 2 hr or more.
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公开(公告)号:JPH1087620A
公开(公告)日:1998-04-07
申请号:JP22346097
申请日:1997-08-20
Applicant: BASF AG
Inventor: JULIUS MANFRED DR , HERMELING DIETER DR , SIEGEL HARDO DR , HARDER WOLFGANG DR
IPC: B01J31/02 , C07B61/00 , C07D211/74
Abstract: PROBLEM TO BE SOLVED: To provide a method, esp. continuous method, for affording 2,2,6,6- tetramethylpiperidin-4-one (TAA) in high yield and also in a shortened time under reduced labor. SOLUTION: The objective 2,2,6,6-tetramethylpiperidin-4-one (TTA) is obtained by reaction of mixture of acetone and/or acetone condensate and ammonia in the molar ratio of (20:1) to (3:1) at 50-130 deg.C in the presence of dimethyl sulfate at 0.5-5mol% based on the acetone.
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公开(公告)号:DE19644770A1
公开(公告)日:1998-04-30
申请号:DE19644770
申请日:1996-10-28
Applicant: BASF AG
Inventor: JULIUS MANFRED DR
IPC: C07D211/58 , C07D211/72
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公开(公告)号:DE19606846A1
公开(公告)日:1997-08-28
申请号:DE19606846
申请日:1996-02-23
Applicant: BASF AG
Inventor: JULIUS MANFRED DR , ETTL ROLAND DR , GUENTHER WOLFGANG DR , GREINDL THOMAS DR
IPC: C07C235/88 , C08F8/30 , C10L1/22 , C10L1/224 , C10L1/238 , C10L1/2383 , C10L1/2387 , C10L10/00 , C10M133/16 , C10M133/52 , C07D305/12 , C08F8/32 , C10M133/56 , C10M149/00
Abstract: Polyalkylamine derivatives of formula ZCH2NH2-nHn (I) are new. (where, n = 0 or 1; z = polyalkyl residue of molecular weight 150-40000; Y = residue of formula (IIa) or (IIb); R, R1 and R2 = H, optionally substituted alk(en)yl, alkinyl, and optionally substituted cycloalkyl, aryl(alkyl) having heteroatom(s); A = alkylene imine residues of formula (III); m = 0-10; Alk = optionally substituted alkylene; R3 = H, alk(en)yl, alkinyl, or aryl or when Y is a residue of formula (IIa) keto residue of formula (IVa); in (IVa): R = as above or when Y = group of formula (IIb), is a cyano residue of formula (IVb) (where, R1 and R2 = as above) or when n = 0 one of the residues Y is optionally a polyoxyalkylene residue (V) (where, q = 1-30; Alk = as above; and E = H or 1-6C alkyl). Preparation of the derivatives is also claimed. Also claimed are lubricant and fuel compositions containing the above derivatives.
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公开(公告)号:ES2234045T3
公开(公告)日:2005-06-16
申请号:ES98103807
申请日:1998-03-04
Applicant: BASF AG
Inventor: VOIT GUIDO DR , WITZEL TOM DR , JULIUS MANFRED DR
IPC: C07D211/12 , B01J21/04 , B01J21/06 , B01J21/08 , B01J31/02 , C07B61/00 , C07D211/58
Abstract: EN EL PROCEDIMIENTO PARA LA PREPARACION DE 4 - AMINO - 2,2,6,6 - TETRAMETIL - PIPERIDINA (TAD) EN UN PRIMER PASO REACCIONA LA 2,2,6,6 - TETRAMETIL - PIPERIDIN - 4 - ONA (TAA) CON AMONIACO EN PRESENCIA DE UN A) CATALIZADOR DE OXIDO METALICO ACIDO O B) CATALIZADORES ACIDOS SOLIDOS, QUE SON PRACTICAMENTE INSOLUBLES EN AGUA, DANDO TAA - IMINA; PARA ELLO EN B) SE EXTRAEN INTERCAMBIADORES IONICOS INORGANICOS E ORGANICOS EN FORMA DE AMONIACO. EN UN SEGUNDO PASO SE HIDROGENA LA TAA - IMINA EN PRESENCIA DE UN CATALIZADOR DE HIDROGENACION.
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