GB844448A - Reductive aminolysis process - Google Patents
Reductive aminolysis processInfo
- Publication number
- GB844448A GB844448A GB3072456A GB3072456A GB844448A GB 844448 A GB844448 A GB 844448A GB 3072456 A GB3072456 A GB 3072456A GB 3072456 A GB3072456 A GB 3072456A GB 844448 A GB844448 A GB 844448A
- Authority
- GB
- United Kingdom
- Prior art keywords
- amines
- corn
- sugar
- hydrogen
- under
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 238000007098 aminolysis reaction Methods 0.000 title abstract 2
- 230000002829 reductive effect Effects 0.000 title abstract 2
- 238000000034 method Methods 0.000 title 1
- 240000008042 Zea mays Species 0.000 abstract 4
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 abstract 4
- 235000002017 Zea mays subsp mays Nutrition 0.000 abstract 4
- 235000005822 corn Nutrition 0.000 abstract 4
- 150000005846 sugar alcohols Polymers 0.000 abstract 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 abstract 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 3
- 150000001412 amines Chemical class 0.000 abstract 3
- -1 heterocyclic nitrogen compounds Chemical class 0.000 abstract 3
- 239000001257 hydrogen Substances 0.000 abstract 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 abstract 2
- 241000609240 Ambelania acida Species 0.000 abstract 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 2
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 abstract 2
- 239000010905 bagasse Substances 0.000 abstract 2
- 239000003054 catalyst Substances 0.000 abstract 2
- 238000006243 chemical reaction Methods 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 238000005984 hydrogenation reaction Methods 0.000 abstract 2
- 235000013379 molasses Nutrition 0.000 abstract 2
- 239000006188 syrup Substances 0.000 abstract 2
- 235000020357 syrup Nutrition 0.000 abstract 2
- BKMMTJMQCTUHRP-UHFFFAOYSA-N 2-aminopropan-1-ol Chemical compound CC(N)CO BKMMTJMQCTUHRP-UHFFFAOYSA-N 0.000 abstract 1
- FBEHFRAORPEGFH-UHFFFAOYSA-N Allyxycarb Chemical compound CNC(=O)OC1=CC(C)=C(N(CC=C)CC=C)C(C)=C1 FBEHFRAORPEGFH-UHFFFAOYSA-N 0.000 abstract 1
- 241000219310 Beta vulgaris subsp. vulgaris Species 0.000 abstract 1
- 241000207199 Citrus Species 0.000 abstract 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 abstract 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 abstract 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 abstract 1
- 239000004386 Erythritol Substances 0.000 abstract 1
- UNXHWFMMPAWVPI-UHFFFAOYSA-N Erythritol Natural products OCC(O)C(O)CO UNXHWFMMPAWVPI-UHFFFAOYSA-N 0.000 abstract 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical class NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 abstract 1
- 229920002488 Hemicellulose Polymers 0.000 abstract 1
- 229930195725 Mannitol Natural products 0.000 abstract 1
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 abstract 1
- 240000000111 Saccharum officinarum Species 0.000 abstract 1
- 235000007201 Saccharum officinarum Nutrition 0.000 abstract 1
- 244000061456 Solanum tuberosum Species 0.000 abstract 1
- 235000002595 Solanum tuberosum Nutrition 0.000 abstract 1
- 235000021536 Sugar beet Nutrition 0.000 abstract 1
- 238000010521 absorption reaction Methods 0.000 abstract 1
- 150000001298 alcohols Chemical class 0.000 abstract 1
- 150000001408 amides Chemical class 0.000 abstract 1
- 229910021529 ammonia Inorganic materials 0.000 abstract 1
- 150000003974 aralkylamines Chemical class 0.000 abstract 1
- 150000004982 aromatic amines Chemical class 0.000 abstract 1
- 239000006227 byproduct Substances 0.000 abstract 1
- 235000020971 citrus fruits Nutrition 0.000 abstract 1
- 235000012343 cottonseed oil Nutrition 0.000 abstract 1
- 229960002887 deanol Drugs 0.000 abstract 1
- 239000012972 dimethylethanolamine Substances 0.000 abstract 1
- UNXHWFMMPAWVPI-ZXZARUISSA-N erythritol Chemical compound OC[C@H](O)[C@H](O)CO UNXHWFMMPAWVPI-ZXZARUISSA-N 0.000 abstract 1
- 235000019414 erythritol Nutrition 0.000 abstract 1
- 229940009714 erythritol Drugs 0.000 abstract 1
- 150000002171 ethylene diamines Chemical class 0.000 abstract 1
- 229940012017 ethylenediamine Drugs 0.000 abstract 1
- 150000004676 glycans Polymers 0.000 abstract 1
- 235000011187 glycerol Nutrition 0.000 abstract 1
- 150000002334 glycols Chemical class 0.000 abstract 1
- 229960004903 invert sugar Drugs 0.000 abstract 1
- 229920005610 lignin Polymers 0.000 abstract 1
- 239000000594 mannitol Substances 0.000 abstract 1
- 235000010355 mannitol Nutrition 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 150000002825 nitriles Chemical class 0.000 abstract 1
- 229910017464 nitrogen compound Inorganic materials 0.000 abstract 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 1
- 150000004885 piperazines Chemical class 0.000 abstract 1
- 239000005017 polysaccharide Substances 0.000 abstract 1
- 150000004804 polysaccharides Polymers 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 239000000047 product Substances 0.000 abstract 1
- 239000000376 reactant Substances 0.000 abstract 1
- 150000003335 secondary amines Chemical class 0.000 abstract 1
- 239000000600 sorbitol Substances 0.000 abstract 1
- 235000010356 sorbitol Nutrition 0.000 abstract 1
- 239000010902 straw Substances 0.000 abstract 1
- 229940066765 systemic antihistamines substituted ethylene diamines Drugs 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/02—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements
- C07D295/027—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements containing only one hetero ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/02—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/02—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements
- C07D295/023—Preparation; Separation; Stabilisation; Use of additives
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US57331456A | 1956-03-23 | 1956-03-23 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB844448A true GB844448A (en) | 1960-08-10 |
Family
ID=24291468
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB3072456A Expired GB844448A (en) | 1956-03-23 | 1956-10-09 | Reductive aminolysis process |
Country Status (5)
| Country | Link |
|---|---|
| BE (1) | BE554427A (forum.php) |
| CH (1) | CH363656A (forum.php) |
| FR (1) | FR1189879A (forum.php) |
| GB (1) | GB844448A (forum.php) |
| NL (1) | NL103288C (forum.php) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4070530A (en) * | 1975-10-30 | 1978-01-24 | Monsanto Company | Catalytic amination of polymeric polyols and resulting amino substituted polymers |
| US4540821A (en) * | 1981-01-26 | 1985-09-10 | Texaco Inc. | Aminopolyols from sugars |
| WO2009027248A1 (de) * | 2007-08-29 | 2009-03-05 | Basf Se | Verfahren zur herstellung von aminen aus glycerin |
| US20100311973A1 (en) * | 2007-08-29 | 2010-12-09 | Basf Se | Method for producing amines from sugar alcohols |
| EP3290401A1 (en) | 2016-08-30 | 2018-03-07 | Taminco bvba | N-substituted acyclic ethylene diamines |
-
0
- NL NL103288D patent/NL103288C/xx active
- BE BE554427D patent/BE554427A/xx unknown
-
1956
- 1956-10-09 GB GB3072456A patent/GB844448A/en not_active Expired
- 1956-11-24 FR FR1189879D patent/FR1189879A/fr not_active Expired
- 1956-12-04 CH CH4028356A patent/CH363656A/fr unknown
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4070530A (en) * | 1975-10-30 | 1978-01-24 | Monsanto Company | Catalytic amination of polymeric polyols and resulting amino substituted polymers |
| US4540821A (en) * | 1981-01-26 | 1985-09-10 | Texaco Inc. | Aminopolyols from sugars |
| WO2009027248A1 (de) * | 2007-08-29 | 2009-03-05 | Basf Se | Verfahren zur herstellung von aminen aus glycerin |
| CN101842345A (zh) * | 2007-08-29 | 2010-09-22 | 巴斯夫欧洲公司 | 由甘油生产胺的方法 |
| US20100311973A1 (en) * | 2007-08-29 | 2010-12-09 | Basf Se | Method for producing amines from sugar alcohols |
| RU2480449C2 (ru) * | 2007-08-29 | 2013-04-27 | Басф Се | Способ получения аминов из глицерина |
| US9067863B2 (en) * | 2007-08-29 | 2015-06-30 | Basf Se | Method for producing amines from sugar alcohols |
| EP3290401A1 (en) | 2016-08-30 | 2018-03-07 | Taminco bvba | N-substituted acyclic ethylene diamines |
Also Published As
| Publication number | Publication date |
|---|---|
| CH363656A (fr) | 1962-08-15 |
| FR1189879A (fr) | 1959-10-07 |
| NL103288C (forum.php) | |
| BE554427A (forum.php) |
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