Process for the reductive amination of halogen-containing substrates
원문보기
IPC분류정보
국가/구분
United States(US) Patent
등록
국제특허분류(IPC7판)
A01N-037/42
C07B-043/04
C07C-209/26
C07C-211/29
C07C-249/04
출원번호
US-0523864
(2015-11-04)
등록번호
US-10173961
(2019-01-08)
우선권정보
EP-14191761 (2014-11-04)
국제출원번호
PCT/EP2015/075734
(2015-11-04)
국제공개번호
WO2016/071410
(2016-05-12)
발명자
/ 주소
Moonen, Kristof
Dumoleijn, Kim
Prati, Laura
Villa, Alberto
출원인 / 주소
Taminco BVBA
대리인 / 주소
Carmen, Dennis V.
인용정보
피인용 횟수 :
0인용 특허 :
8
초록▼
Disclosed is a process for performing a reductive amination of a first functional group in an organic feed substrate, which feed substrate comprises at least one further functional group containing a halogen atom, wherein the halogen atom is selected from the list consisting of chlorine, bromine, io
Disclosed is a process for performing a reductive amination of a first functional group in an organic feed substrate, which feed substrate comprises at least one further functional group containing a halogen atom, wherein the halogen atom is selected from the list consisting of chlorine, bromine, iodine, and combinations thereof, in the presence of hydrogen and a heterogeneous catalyst comprising at least one metal from the list of Pd, Pt, Rh, Ir, and Ru, and in absence of any catalytic amount of any second metal from the list consisting of Ag, Ni, Co, Sn, Bi, Cu, Au, and combinations thereof. The process is preferably applied for the reductive amination of 2-chloro-benzaldehyde to form 2-chloro-benzyldimethylamine, as an intermediate in the production of active agrochemical compounds and microbicides of the methoximinophenylglyoxylic ester series.
대표청구항▼
1. A process for performing a reductive amination of a chloro benzaldehyde organic feed substrate in the presence of hydrogen and a heterogeneous catalyst comprising palladium or platinum, and in absence of a catalytic amount of any second metal selected from the list consisting of silver, nickel, c
1. A process for performing a reductive amination of a chloro benzaldehyde organic feed substrate in the presence of hydrogen and a heterogeneous catalyst comprising palladium or platinum, and in absence of a catalytic amount of any second metal selected from the list consisting of silver, nickel, cobalt, tin, bismuth, copper, gold, and combinations thereof, whereby the heterogeneous catalyst has been heat-treated prior to the reductive amination at a temperature in the range of 100° C. to 600° C. for a period of at least one hour. 2. The process according to claim 1, comprising reductively aminating ortho-chloro-benzaldehyde with dimethyl amine in the presence of hydrogen and said catalyst to produce ortho-chloro benzyl dimethyl amine. 3. The process according to claim 1, wherein the reductive amination is performed in two steps, in the first step reacting the substrate, containing as the first functional group an aldehyde, with a nitrogen containing compound, and in the subsequent step introducing hydrogen and the catalyst. 4. The process according to claim 1, wherein the heterogeneous catalyst comprises the first metal at a concentration in the range of 0.1-10.0% by weight, based on the total weight of the catalyst and the second metal or combinations thereof at a concentration of at most 0.1% by weight, based on the total weight of the catalyst. 5. The process according to claim 1, wherein the heterogeneous catalyst has been heat treated at a temperature of at least 200° C. for at least 2 hours. 6. The process according to claim 1, wherein the heat treatment of the heterogeneous catalyst is performed by exposure of the catalyst to a flow of nitrogen at a WWH in the range of from 0.0200 to 2.0000 h−1. 7. The process according to claim 6, wherein the heterogeneous catalyst at the start of the heat-treatment contains at most 5% wt free water. 8. The process according to claim 1, wherein the heterogeneous catalyst has been dried prior to the heat-treatment. 9. The process according to claim 1, wherein the heat treatment is performed in the presence of a liquid comprising the feed substrate, a solvent, or mixtures thereof. 10. The process according to claim 1, wherein the heterogeneous catalyst has a support comprising carbon, alumina, silica, zeolite, clay, porous polymer or a hybrid polymer. 11. The process according to claim 1, wherein the heterogeneous catalyst has an average metal particle size in the range of 2 to 20 nm. 12. The process according to claim 1, wherein the heterogeneous catalyst has been pre-reduced after the heat treatment and prior to the step of contacting the catalyst with the organic feed substrate by subjecting the catalyst to a hydrogen partial pressure of at least 5 bar absolute, during a period of at least 30 minutes and at a temperature of at least 120° C. 13. The process according to claim 1, wherein at least 80% of chlorine atoms on the feed substrate are retained after the conversion. 14. The process according to claim 1, wherein the reductive amination is performed at an H2 partial pressure in the range of 0.01-250 bar gauge. 15. The process according to claim 1, wherein the reductive amination is performed in the presence of methanol. 16. The process according to claim 1, wherein said process produces ortho-chloro-benzyldimethylamine, further comprising a first step the preparation of making a Grignard reagent from the ortho-chloro-benzyldimethylamine by introducing a magnesium atom between the benzene ring of the ortho-chloro-benzyldimethylamine compound and its chlorine atom, followed by a second step wherein the Grignard reagent is esterified to make a methoximinophenylglyoxylic ester. 17. The process according to claim 16, further comprising the production of a fungicide including the methoximinophenylglyoxylic ester. 18. The process according to claim 17, further including the step of treating a surface with the fungicide containing the methoximinophenylglyoxylic ester. 19. The process according to claim 1, wherein the heterogeneous catalyst has been heat-treated prior to the reductive amination at a temperature in the range of 200° C. to 600° C. for a period of at least two hours. 20. The process according to claim 1, wherein the heterogeneous catalyst has been heat-treated, prior to the reductive amination, at a temperature in the range of 200° C. to 600° C. for a period of at least two hours. 21. The process according to claim 1, wherein the heterogeneous catalyst has been heat-treated prior to the reductive amination under a flow of nitrogen at a WWH rate at least 0.050 h−1. 22. The process according to claim 1, wherein the heterogeneous catalyst has been heat-treated prior to the reductive amination under a flow of nitrogen at a WWH rate at least 0.075 h−1. 23. The process according to claim 1, wherein the heterogeneous catalyst has been heat-treated prior to the reductive amination at a temperature within a range of 200° C. to 600° C. under a flow of nitrogen at a WWH rate at least 0.050 h−1 for at least two hours. 24. The process according to claim 23, wherein the temperature is within a range of 300° C. to 600° C. and the WWH flow of nitrogen is at least 0.120 hr−1. 25. The process according to claim 24, wherein the catalyst is dried at a temperature of less than 100° C. before said heat treatment step sufficient such that the catalyst, at the start of the heat treatment step, contains not more than 10 wt. % free water, based on the weight of the catalyst.
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이 특허에 인용된 특허 (8)
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Deller Klaus (Hainburg DEX) Despeyroux Bertrand (Hanau DEX) Peldszus Erik (Hasselroth DEX) Kleinwaechter Beate (Hanau DEX), Catalyst for the selective hydrogenation of aromatic halonitro compounds to aromatic haloamines and a process for its pr.
Borner,Armin; Dingerdissen,Uwe; Kadyrov,Renat; Riermeier,Thomas; Tararov,Vitali, Method for the production of amines by reductive amination of carbonyl compounds under transfer-hydrogenation conditions.
Cordier Georges (Francheville FRX) Damon Jean-Pierre (Le Touvet FRX) Fouilloux Pierre (Caluire et Cuire FRX) Marion Philippe (Villeurbanne FRX), Raney-type catalysts for the hydrogenation of halonitroaromatic compounds.
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