ES2727436T3 - Preparación de caprolactona, caprolactama, 2,5-tetrahidrofuran-dimetanol, 1,6-hexanodiol o 1,2,6-hexanotriol a partir de 5-hidroximetil-2-furfuraldehído - Google Patents
Preparación de caprolactona, caprolactama, 2,5-tetrahidrofuran-dimetanol, 1,6-hexanodiol o 1,2,6-hexanotriol a partir de 5-hidroximetil-2-furfuraldehído Download PDFInfo
- Publication number
- ES2727436T3 ES2727436T3 ES11712049T ES11712049T ES2727436T3 ES 2727436 T3 ES2727436 T3 ES 2727436T3 ES 11712049 T ES11712049 T ES 11712049T ES 11712049 T ES11712049 T ES 11712049T ES 2727436 T3 ES2727436 T3 ES 2727436T3
- Authority
- ES
- Spain
- Prior art keywords
- hexanediol
- catalyst
- hexanedriol
- tetrahydrofuran
- hydrogenation
- 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.)
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- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 title claims abstract description 77
- NOEGNKMFWQHSLB-UHFFFAOYSA-N 5-hydroxymethylfurfural Chemical compound OCC1=CC=C(C=O)O1 NOEGNKMFWQHSLB-UHFFFAOYSA-N 0.000 title claims abstract description 46
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 title claims abstract description 46
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 title claims description 50
- 238000002360 preparation method Methods 0.000 title description 16
- 238000005984 hydrogenation reaction Methods 0.000 claims abstract description 72
- 238000004519 manufacturing process Methods 0.000 claims abstract description 20
- 150000001875 compounds Chemical class 0.000 claims abstract description 11
- YCZZQSFWHFBKMU-UHFFFAOYSA-N [5-(hydroxymethyl)oxolan-2-yl]methanol Chemical compound OCC1CCC(CO)O1 YCZZQSFWHFBKMU-UHFFFAOYSA-N 0.000 claims abstract description 3
- 239000003054 catalyst Substances 0.000 claims description 94
- 238000000034 method Methods 0.000 claims description 54
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 43
- 238000006243 chemical reaction Methods 0.000 claims description 40
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 31
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 27
- 239000000377 silicon dioxide Substances 0.000 claims description 20
- 239000000203 mixture Substances 0.000 claims description 15
- 229930091371 Fructose Natural products 0.000 claims description 13
- 239000005715 Fructose Substances 0.000 claims description 13
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 claims description 13
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims description 12
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 claims description 12
- 239000008103 glucose Substances 0.000 claims description 11
- 239000007868 Raney catalyst Substances 0.000 claims description 10
- 229910000564 Raney nickel Inorganic materials 0.000 claims description 10
- ROTONRWJLXYJBD-UHFFFAOYSA-N oxan-2-ylmethanol Chemical compound OCC1CCCCO1 ROTONRWJLXYJBD-UHFFFAOYSA-N 0.000 claims description 10
- JGDFBJMWFLXCLJ-UHFFFAOYSA-N copper chromite Chemical compound [Cu]=O.[Cu]=O.O=[Cr]O[Cr]=O JGDFBJMWFLXCLJ-UHFFFAOYSA-N 0.000 claims description 9
- 239000002585 base Substances 0.000 claims description 8
- WCJIUQVBQSTBDE-UHFFFAOYSA-N [Rh].[Re] Chemical compound [Rh].[Re] WCJIUQVBQSTBDE-UHFFFAOYSA-N 0.000 claims description 7
- 239000003444 phase transfer catalyst Substances 0.000 claims description 7
- WYURNTSHIVDZCO-UHFFFAOYSA-N tetrahydrofuran Substances C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 7
- 229920002472 Starch Polymers 0.000 claims description 6
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- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 4
- 239000001913 cellulose Substances 0.000 claims description 4
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- 150000005621 tetraalkylammonium salts Chemical class 0.000 claims 1
- ZWVMLYRJXORSEP-UHFFFAOYSA-N 1,2,6-Hexanetriol Chemical compound OCCCCC(O)CO ZWVMLYRJXORSEP-UHFFFAOYSA-N 0.000 abstract 1
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- 239000002105 nanoparticle Substances 0.000 description 10
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- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 10
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- -1 cyclohexane Chemical class 0.000 description 6
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 6
- 229910052763 palladium Inorganic materials 0.000 description 6
- 229910052702 rhenium Inorganic materials 0.000 description 6
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- SLXKOJJOQWFEFD-UHFFFAOYSA-N 6-aminohexanoic acid Chemical compound NCCCCCC(O)=O SLXKOJJOQWFEFD-UHFFFAOYSA-N 0.000 description 3
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- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 1
- 239000005751 Copper oxide Substances 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- 108010073178 Glucan 1,4-alpha-Glucosidase Proteins 0.000 description 1
- 102100022624 Glucoamylase Human genes 0.000 description 1
- 125000001176 L-lysyl group Chemical class [H]N([H])[C@]([H])(C(=O)[*])C([H])([H])C([H])([H])C([H])([H])C(N([H])[H])([H])[H] 0.000 description 1
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 1
- QLZHNIAADXEJJP-UHFFFAOYSA-N Phenylphosphonic acid Chemical compound OP(O)(=O)C1=CC=CC=C1 QLZHNIAADXEJJP-UHFFFAOYSA-N 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- 108700040099 Xylose isomerases Proteins 0.000 description 1
- DGEZNRSVGBDHLK-UHFFFAOYSA-N [1,10]phenanthroline Chemical compound C1=CN=C2C3=NC=CC=C3C=CC2=C1 DGEZNRSVGBDHLK-UHFFFAOYSA-N 0.000 description 1
- QLSOZHFOFHARBJ-UHFFFAOYSA-N [3-(diphenylphosphanylmethyl)phenyl]methyl-diphenylphosphane Chemical compound C=1C=CC(CP(C=2C=CC=CC=2)C=2C=CC=CC=2)=CC=1CP(C=1C=CC=CC=1)C1=CC=CC=C1 QLSOZHFOFHARBJ-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001299 aldehydes Chemical group 0.000 description 1
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 150000004703 alkoxides Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 108090000637 alpha-Amylases Proteins 0.000 description 1
- 102000004139 alpha-Amylases Human genes 0.000 description 1
- 229940024171 alpha-amylase Drugs 0.000 description 1
- 150000004645 aluminates Chemical class 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 235000019418 amylase Nutrition 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- KXHPPCXNWTUNSB-UHFFFAOYSA-M benzyl(trimethyl)azanium;chloride Chemical compound [Cl-].C[N+](C)(C)CC1=CC=CC=C1 KXHPPCXNWTUNSB-UHFFFAOYSA-M 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 238000001354 calcination Methods 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 229910000420 cerium oxide Inorganic materials 0.000 description 1
- 229920001429 chelating resin Polymers 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 230000009194 climbing Effects 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 229910052681 coesite Inorganic materials 0.000 description 1
- 230000002860 competitive effect Effects 0.000 description 1
- 239000002361 compost Substances 0.000 description 1
- 150000004696 coordination complex Chemical class 0.000 description 1
- 229910000431 copper oxide Inorganic materials 0.000 description 1
- TVZPLCNGKSPOJA-UHFFFAOYSA-N copper zinc Chemical compound [Cu].[Zn] TVZPLCNGKSPOJA-UHFFFAOYSA-N 0.000 description 1
- 229910052593 corundum Inorganic materials 0.000 description 1
- 229910052906 cristobalite Inorganic materials 0.000 description 1
- 229930007927 cymene Natural products 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 239000012973 diazabicyclooctane Substances 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000000855 fermentation Methods 0.000 description 1
- 230000004151 fermentation Effects 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 235000003869 genetically modified organism Nutrition 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical compound CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 description 1
- 238000009905 homogeneous catalytic hydrogenation reaction Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 238000007327 hydrogenolysis reaction Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 238000012432 intermediate storage Methods 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- GRWIABMEEKERFV-UHFFFAOYSA-N methanol;oxolane Chemical compound OC.C1CCOC1 GRWIABMEEKERFV-UHFFFAOYSA-N 0.000 description 1
- 230000002906 microbiologic effect Effects 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 150000002772 monosaccharides Chemical group 0.000 description 1
- JHUJKLXQENRSHH-UHFFFAOYSA-N n,n-dimethyl-1-phenylmethanamine;n-methyl-1-phenylmethanamine Chemical compound CNCC1=CC=CC=C1.CN(C)CC1=CC=CC=C1 JHUJKLXQENRSHH-UHFFFAOYSA-N 0.000 description 1
- GZPHDJXXLCGMTI-UHFFFAOYSA-N n-methyl-1-[3-(methylaminomethyl)phenyl]methanamine Chemical compound CNCC1=CC=CC(CNC)=C1 GZPHDJXXLCGMTI-UHFFFAOYSA-N 0.000 description 1
- 210000003739 neck Anatomy 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- BMMGVYCKOGBVEV-UHFFFAOYSA-N oxo(oxoceriooxy)cerium Chemical compound [Ce]=O.O=[Ce]=O BMMGVYCKOGBVEV-UHFFFAOYSA-N 0.000 description 1
- HFPZCAJZSCWRBC-UHFFFAOYSA-N p-cymene Chemical compound CC(C)C1=CC=C(C)C=C1 HFPZCAJZSCWRBC-UHFFFAOYSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- WQIQNKQYEUMPBM-UHFFFAOYSA-N pentamethylcyclopentadiene Chemical compound CC1C(C)=C(C)C(C)=C1C WQIQNKQYEUMPBM-UHFFFAOYSA-N 0.000 description 1
- XRBCRPZXSCBRTK-UHFFFAOYSA-N phosphonous acid Chemical class OPO XRBCRPZXSCBRTK-UHFFFAOYSA-N 0.000 description 1
- 150000008300 phosphoramidites Chemical class 0.000 description 1
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 230000006340 racemization Effects 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 238000004626 scanning electron microscopy Methods 0.000 description 1
- 238000001350 scanning transmission electron microscopy Methods 0.000 description 1
- 239000012056 semi-solid material Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- LKZMBDSASOBTPN-UHFFFAOYSA-L silver carbonate Substances [Ag].[O-]C([O-])=O LKZMBDSASOBTPN-UHFFFAOYSA-L 0.000 description 1
- 229910001958 silver carbonate Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- NYCVSSWORUBFET-UHFFFAOYSA-M sodium;bromite Chemical compound [Na+].[O-]Br=O NYCVSSWORUBFET-UHFFFAOYSA-M 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910052682 stishovite Inorganic materials 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 125000005207 tetraalkylammonium group Chemical class 0.000 description 1
- 238000009901 transfer hydrogenation reaction Methods 0.000 description 1
- 238000004627 transmission electron microscopy Methods 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- 229910052905 tridymite Inorganic materials 0.000 description 1
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 1
- COIOYMYWGDAQPM-UHFFFAOYSA-N tris(2-methylphenyl)phosphane Chemical compound CC1=CC=CC=C1P(C=1C(=CC=CC=1)C)C1=CC=CC=C1C COIOYMYWGDAQPM-UHFFFAOYSA-N 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
- 229910001845 yogo sapphire Inorganic materials 0.000 description 1
- 150000003754 zirconium Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D313/00—Heterocyclic compounds containing rings of more than six members having one oxygen atom as the only ring hetero atom
- C07D313/02—Seven-membered rings
- C07D313/04—Seven-membered rings not condensed with other rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/132—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D201/00—Preparation, separation, purification or stabilisation of unsubstituted lactams
- C07D201/02—Preparation of lactams
- C07D201/08—Preparation of lactams from carboxylic acids or derivatives thereof, e.g. hydroxy carboxylic acids, lactones or nitriles
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
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)
- Catalysts (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
- Furan Compounds (AREA)
- Pyrane Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP10163881A EP2390247A1 (en) | 2010-05-26 | 2010-05-26 | Preparation of caprolactone, caprolactam, 2,5-tetrahydrofuran dimethanol, 1,6-hexanediol or 1,2,6-hexanetriol from 5-hydroxymethyl-2-furfuraldehyde |
| PCT/NL2011/050200 WO2011149339A1 (en) | 2010-05-26 | 2011-03-23 | Preparation of caprolactone, caprolactam, 2,5-tetrahydrofuran-dimethanol, 1,6-hexanediol or 1,2,6-hexanetriol from 5-hydroxymethyl-2-furfuraldehyde |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2727436T3 true ES2727436T3 (es) | 2019-10-16 |
Family
ID=42797300
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES11712049T Active ES2727436T3 (es) | 2010-05-26 | 2011-03-23 | Preparación de caprolactona, caprolactama, 2,5-tetrahidrofuran-dimetanol, 1,6-hexanodiol o 1,2,6-hexanotriol a partir de 5-hidroximetil-2-furfuraldehído |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US9199961B2 (https=) |
| EP (2) | EP2390247A1 (https=) |
| JP (1) | JP6327853B2 (https=) |
| CN (1) | CN103228626B (https=) |
| BR (1) | BR112012029996B1 (https=) |
| CA (1) | CA2800797C (https=) |
| ES (1) | ES2727436T3 (https=) |
| WO (1) | WO2011149339A1 (https=) |
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| WO2011149839A1 (en) | 2010-05-24 | 2011-12-01 | Tandus Flooring, Inc. | Textile backing formed from recycled materials |
| EP2390247A1 (en) | 2010-05-26 | 2011-11-30 | Netherlands Organisation for Scientific Research (Advanced Chemical Technologies for Sustainability) | Preparation of caprolactone, caprolactam, 2,5-tetrahydrofuran dimethanol, 1,6-hexanediol or 1,2,6-hexanetriol from 5-hydroxymethyl-2-furfuraldehyde |
| US8884036B2 (en) | 2011-12-30 | 2014-11-11 | E I Du Pont De Nemours And Company | Production of hydroxymethylfurfural from levoglucosenone |
| EP2797866A4 (en) * | 2011-12-30 | 2015-08-05 | Du Pont | PROCESS FOR THE PREPARATION OF 1,6-HEXANEDIOL |
| US8865940B2 (en) | 2011-12-30 | 2014-10-21 | E I Du Pont De Nemours And Company | Process for preparing 1,6-hexanediol |
| BR112014015994A2 (pt) * | 2011-12-30 | 2018-05-22 | Du Pont | processo. |
| JP2015503569A (ja) * | 2011-12-30 | 2015-02-02 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニーＥ．Ｉ．Ｄｕ Ｐｏｎｔ Ｄｅ Ｎｅｍｏｕｒｓ Ａｎｄ Ｃｏｍｐａｎｙ | ヘキサンジオールを生成するための方法 |
| US8889912B2 (en) | 2011-12-30 | 2014-11-18 | E I Du Pont De Nemours And Company | Process for preparing 1,6-hexanediol |
| AR089707A1 (es) * | 2012-01-18 | 2014-09-10 | Rennovia Inc | Proceso para la produccion de hexametilendiamina a partir de materiales que contienen carbohidratos y compuestos intermedios para la misma |
| JP6168044B2 (ja) * | 2012-03-09 | 2017-07-26 | 宇部興産株式会社 | テトラヒドロフラン化合物の製造方法 |
| EP2644585A1 (en) | 2012-03-30 | 2013-10-02 | Rheinisch-Westfälisch-Technische Hochschule Aachen | Method for the production of aliphatic alcohols and/or their ethers |
| US8846985B2 (en) | 2012-04-27 | 2014-09-30 | E I Du Pont De Nemours And Company | Production of alpha, omega-diols |
| US9018423B2 (en) | 2012-04-27 | 2015-04-28 | E I Du Pont De Nemours And Company | Production of alpha, omega-diols |
| US8859826B2 (en) | 2012-04-27 | 2014-10-14 | E I Du Pont De Nemours And Company | Production of alpha, omega-diols |
| AU2013274530B2 (en) | 2012-06-11 | 2017-09-28 | Rennovia, Inc. | Process for production of adipic acid from 1,6-hexanediol |
| FR2995897B1 (fr) * | 2012-09-27 | 2014-10-10 | Roquette Freres | Procede de synthese de 2,5-di(hydroxymethyl)furane et de 2,5-di(hydroxymethyl)tetrahydrofurane par hydrogenation selective de furane-2,5-dialdehyde |
| WO2014152366A1 (en) * | 2013-03-14 | 2014-09-25 | Pronghorn Renewables Llc | Method and catalyst for the production of alcohols, diols, cyclic ethers and other products from pentose and hexose sugars |
| CN105658700B (zh) * | 2013-10-22 | 2018-07-10 | 英派尔科技开发有限公司 | 用于产生尼龙6的化合物和方法 |
| WO2015060827A1 (en) * | 2013-10-22 | 2015-04-30 | Empire Technology Development Llc | Methods and compounds for producing nylon 6,6 |
| CN105658616A (zh) | 2013-10-25 | 2016-06-08 | 英派尔科技开发有限公司 | 产生二羰基化合物的方法 |
| EA201691459A1 (ru) | 2014-01-27 | 2016-12-30 | Ренновия Инк. | Преобразование фруктозосодержащего исходного сырья в hmf-содержащий продукт |
| RU2016141809A (ru) * | 2014-04-10 | 2018-05-10 | Арчер Дэниелс Мидлэнд Компани | Синтез R-глюкозидов сахароспиртов, восстановленных сахароспиртов и фурановых производных восстановленных сахароспиртов |
| JP2017513841A (ja) * | 2014-04-10 | 2017-06-01 | アーチャー−ダニエルズ−ミッドランド カンパニー | 還元糖アルコール、フラン誘導体の合成 |
| CN111205173A (zh) * | 2014-05-12 | 2020-05-29 | 威尔迪亚公司 | 来自生物质精制的经氧化分子的氢化 |
| WO2016043589A1 (en) * | 2014-09-19 | 2016-03-24 | Rijksuniversiteit Groningen | Method for reducing hydroxymethylfurfural (hmf) |
| CN107074761B (zh) * | 2014-10-30 | 2020-04-14 | 东丽株式会社 | ε-己内酰胺的制造方法 |
| JP2017537920A (ja) | 2014-12-02 | 2017-12-21 | レノビア インコーポレイテッド | ５−ヒドロキシメチルフルフラールから２，５−ビスヒドロキシメチルフラン、２，５−ビス−ヒドロキシメチルテトラヒドロフラン、１，６−ヘキサンジオールおよび１，２，６−ヘキサントリオールを生成する工程 |
| CN104591369A (zh) * | 2014-12-23 | 2015-05-06 | 南京林业大学 | 一种用于促使过氧化氢产生羟基自由基的复合药剂及其应用 |
| GB201506701D0 (en) | 2015-04-20 | 2015-06-03 | Univ York | Method for converting waste lignocellulosic materials derived from converting lignocellulose to ethanol into levoglucosenone |
| CN106866360B (zh) * | 2015-12-10 | 2020-09-04 | 中国科学院大连化学物理研究所 | 一种5-羟甲基糠醛催化转化制备1,6-己二醇的方法 |
| EP3402787A4 (en) | 2016-01-13 | 2019-11-27 | Stora Enso Oyj | PROCESS FOR THE PREPARATION OF 2,5-FURANDIC ACETIC ACID AND INTERMEDIATES AND DERIVATIVES THEREOF |
| EP3652161A1 (en) | 2017-07-12 | 2020-05-20 | Stora Enso Oyj | Purified 2,5-furandicarboxylic acid pathway products |
| CN111777578B (zh) * | 2020-07-15 | 2022-06-24 | 烟台大学 | 5-羟甲基糠醛加氢制备2,5-二羟甲基四氢呋喃的方法 |
| DE102021209234A1 (de) | 2021-08-23 | 2023-02-23 | Continental Reifen Deutschland Gmbh | Verfahren zum Herstellen von nachhaltigeren Verbundmaterialien zur Verwendung bei der Herstellung von Fahrzeugreifen |
| CN117229123A (zh) * | 2023-08-14 | 2023-12-15 | 中科国生(杭州)科技有限公司 | 一种1,2,6-己三醇的制备方法 |
| KR20250076198A (ko) * | 2023-11-22 | 2025-05-29 | 한국생산기술연구원 | 루테늄 담지 알루미나 촉매, 그의 제조방법 및 그를 이용한 연속식 테트라하이드로퓨란 다이메탄올(thfdm) 제조장치 |
| CN120754873B (zh) * | 2025-09-10 | 2025-12-02 | 陕西开达化工有限责任公司 | 糠醛加氢胺化制糠胺催化剂及其制备方法 |
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| US3025306A (en) | 1960-05-31 | 1962-03-13 | Union Carbide Corp | Process for the production of epsiloncaprolactones and carboxylic acids |
| US3317563A (en) | 1963-12-26 | 1967-05-02 | Celanese Corp | Preparation of epsilon-caprolactone |
| JPS5268422A (en) | 1975-12-03 | 1977-06-07 | Yokogawa Hokushin Electric Corp | Two-color electrostatic recording apparatus |
| JPS5524107A (en) | 1978-08-09 | 1980-02-21 | Asahi Chem Ind Co Ltd | Preparation of lactone |
| JPS5925383B2 (ja) | 1979-03-30 | 1984-06-16 | シャープ株式会社 | 半導体装置 |
| US4324710A (en) * | 1980-10-02 | 1982-04-13 | The Firestone Tire & Rubber Company | Naturally occurring thermoplastic resins as a substitute for various petroleum-derived materials in rubber stocks |
| US4400468A (en) * | 1981-10-05 | 1983-08-23 | Hydrocarbon Research Inc. | Process for producing adipic acid from biomass |
| JPS5925383A (ja) | 1982-07-30 | 1984-02-09 | Nippon Shirika Kogyo Kk | 亜臭素酸およびその塩によるラクトンの製造法 |
| JPS6148509A (ja) | 1984-08-13 | 1986-03-10 | Nippon Steel Corp | 転炉炉口付着物加熱切削除去方法 |
| US5451673A (en) * | 1993-04-23 | 1995-09-19 | The United States Of America As Represented By The Secretary Of Agriculture | Films fabricated from mixtures of pectin and starch |
| DE19510438A1 (de) * | 1995-03-22 | 1996-09-26 | Basf Ag | Verfahren zur Herstellung von 1,4-Butandiol und Tetrahydrofuran aus Furan |
| US6300496B1 (en) * | 1999-10-06 | 2001-10-09 | Union Carbide Chemicals & Plastics Technology Corporation | Processes for producing epsilon caprolactams |
| JP4276406B2 (ja) * | 2002-04-30 | 2009-06-10 | トヨタ自動車株式会社 | アミド化合物およびアミノ化合物の製造方法 |
| BRPI0506942B1 (pt) | 2004-01-19 | 2015-07-28 | Dsm Ip Assets B.V. | Síntese bioquímica de ácido 6-amino capróico |
| JP2008502728A (ja) | 2004-06-10 | 2008-01-31 | ボード、オブ、トラスティーズ、オブ、ミシガン、ステイト、ユニバーシティ | リジンからのカプロラクタムの合成 |
| US7393963B2 (en) * | 2004-12-10 | 2008-07-01 | Archer-Daniels-Midland Company | Conversion of 2,5-(hydroxymethyl)furaldehyde to industrial derivatives, purification of the derivatives, and industrial uses therefor |
| CN101528725A (zh) * | 2006-10-18 | 2009-09-09 | 巴斯夫欧洲公司 | 由二元醇生产内酯的方法 |
| AU2008205169B2 (en) | 2007-01-05 | 2012-02-02 | Novartis Ag | Imidazole derivatives as kinesin spindle protein inhibitors (Eg-5) |
| WO2009154566A1 (en) * | 2008-06-18 | 2009-12-23 | Agency For Science, Technology And Research | Production of hydroxymethylfurfural |
| JP5209426B2 (ja) * | 2008-09-22 | 2013-06-12 | 富士フイルム株式会社 | １，２，４−オキサジアゾール誘導体の製造方法 |
| JP2010208968A (ja) | 2009-03-09 | 2010-09-24 | Daicel Chem Ind Ltd | 表面金固定化触媒によるラクトンの製造方法 |
| EP2390247A1 (en) | 2010-05-26 | 2011-11-30 | Netherlands Organisation for Scientific Research (Advanced Chemical Technologies for Sustainability) | Preparation of caprolactone, caprolactam, 2,5-tetrahydrofuran dimethanol, 1,6-hexanediol or 1,2,6-hexanetriol from 5-hydroxymethyl-2-furfuraldehyde |
-
2010
- 2010-05-26 EP EP10163881A patent/EP2390247A1/en not_active Withdrawn
-
2011
- 2011-03-23 WO PCT/NL2011/050200 patent/WO2011149339A1/en not_active Ceased
- 2011-03-23 EP EP11712049.3A patent/EP2576506B1/en active Active
- 2011-03-23 CN CN201180036114.6A patent/CN103228626B/zh not_active Expired - Fee Related
- 2011-03-23 JP JP2013512556A patent/JP6327853B2/ja not_active Expired - Fee Related
- 2011-03-23 ES ES11712049T patent/ES2727436T3/es active Active
- 2011-03-23 CA CA2800797A patent/CA2800797C/en active Active
- 2011-03-23 BR BR112012029996-4A patent/BR112012029996B1/pt not_active IP Right Cessation
- 2011-03-23 US US13/699,934 patent/US9199961B2/en active Active
Also Published As
| Publication number | Publication date |
|---|---|
| JP6327853B2 (ja) | 2018-05-23 |
| WO2011149339A1 (en) | 2011-12-01 |
| CA2800797C (en) | 2019-04-16 |
| BR112012029996B1 (pt) | 2021-10-26 |
| JP2013531638A (ja) | 2013-08-08 |
| CN103228626A (zh) | 2013-07-31 |
| CN103228626B (zh) | 2016-08-03 |
| US9199961B2 (en) | 2015-12-01 |
| CA2800797A1 (en) | 2011-12-01 |
| US20130137863A1 (en) | 2013-05-30 |
| EP2576506A1 (en) | 2013-04-10 |
| EP2390247A1 (en) | 2011-11-30 |
| BR112012029996A2 (pt) | 2021-05-04 |
| EP2576506B1 (en) | 2019-03-06 |
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