CN104169263B - 在蒸汽存在下由己糖溶液制备5-羟甲基糠醛(hmf) - Google Patents
在蒸汽存在下由己糖溶液制备5-羟甲基糠醛(hmf) Download PDFInfo
- Publication number
- CN104169263B CN104169263B CN201280059056.3A CN201280059056A CN104169263B CN 104169263 B CN104169263 B CN 104169263B CN 201280059056 A CN201280059056 A CN 201280059056A CN 104169263 B CN104169263 B CN 104169263B
- Authority
- CN
- China
- Prior art keywords
- hmf
- hexose
- starting soln
- steam
- fructose
- 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 - Fee Related
Links
- NOEGNKMFWQHSLB-UHFFFAOYSA-N 5-hydroxymethylfurfural Chemical compound OCC1=CC=C(C=O)O1 NOEGNKMFWQHSLB-UHFFFAOYSA-N 0.000 title claims abstract description 81
- RJGBSYZFOCAGQY-UHFFFAOYSA-N hydroxymethylfurfural Natural products COC1=CC=C(C=O)O1 RJGBSYZFOCAGQY-UHFFFAOYSA-N 0.000 title claims abstract description 81
- 150000002402 hexoses Chemical class 0.000 title claims abstract description 41
- 238000000034 method Methods 0.000 claims abstract description 57
- 238000009835 boiling Methods 0.000 claims abstract description 36
- 239000000243 solution Substances 0.000 claims abstract description 17
- 239000007864 aqueous solution Substances 0.000 claims abstract description 11
- 239000003960 organic solvent Substances 0.000 claims abstract description 9
- 238000004821 distillation Methods 0.000 claims abstract description 5
- 229930091371 Fructose Natural products 0.000 claims description 22
- 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 22
- 239000005715 Fructose Substances 0.000 claims description 22
- 229920000570 polyether Polymers 0.000 claims description 18
- 239000002253 acid Substances 0.000 claims description 17
- 238000006243 chemical reaction Methods 0.000 claims description 16
- 239000006200 vaporizer Substances 0.000 claims description 15
- 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 14
- 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 14
- 239000008103 glucose Substances 0.000 claims description 14
- 239000000203 mixture Substances 0.000 claims description 12
- CHTHALBTIRVDBM-UHFFFAOYSA-N furan-2,5-dicarboxylic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)O1 CHTHALBTIRVDBM-UHFFFAOYSA-N 0.000 claims description 10
- 239000012528 membrane Substances 0.000 claims description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 4
- XPFVYQJUAUNWIW-UHFFFAOYSA-N furfuryl alcohol Chemical compound OCC1=CC=CO1 XPFVYQJUAUNWIW-UHFFFAOYSA-N 0.000 claims description 4
- 239000011541 reaction mixture Substances 0.000 claims description 4
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 3
- 238000011144 upstream manufacturing Methods 0.000 claims description 3
- 239000000306 component Substances 0.000 description 28
- 239000006227 byproduct Substances 0.000 description 17
- 239000000126 substance Substances 0.000 description 13
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 10
- 230000015572 biosynthetic process Effects 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- 238000003786 synthesis reaction Methods 0.000 description 7
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 6
- 239000002663 humin Substances 0.000 description 6
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 5
- 125000000217 alkyl group Chemical group 0.000 description 5
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- 125000001118 alkylidene group Chemical group 0.000 description 4
- 150000002170 ethers Chemical class 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 229920001515 polyalkylene glycol Polymers 0.000 description 4
- 238000001256 steam distillation Methods 0.000 description 4
- ZUHZGEOKBKGPSW-UHFFFAOYSA-N tetraglyme Chemical compound COCCOCCOCCOCCOC ZUHZGEOKBKGPSW-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- -1 ethylidene, propylidene Chemical group 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- 238000007171 acid catalysis Methods 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 150000001991 dicarboxylic acids Chemical class 0.000 description 2
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 2
- 238000002955 isolation Methods 0.000 description 2
- 229940098779 methanesulfonic acid Drugs 0.000 description 2
- 235000006408 oxalic acid Nutrition 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000001117 sulphuric acid Substances 0.000 description 2
- 235000011149 sulphuric acid Nutrition 0.000 description 2
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
- DSLRVRBSNLHVBH-UHFFFAOYSA-N 2,5-furandimethanol Chemical compound OCC1=CC=C(CO)O1 DSLRVRBSNLHVBH-UHFFFAOYSA-N 0.000 description 1
- KAZRCBVXUOCTIO-UHFFFAOYSA-N 5-(chloromethyl)furan-2-carbaldehyde Chemical compound ClCC1=CC=C(C=O)O1 KAZRCBVXUOCTIO-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 229920002582 Polyethylene Glycol 600 Polymers 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 239000000010 aprotic solvent Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 229920005601 base polymer Polymers 0.000 description 1
- ZPFKRQXYKULZKP-UHFFFAOYSA-N butylidene Chemical group [CH2+]CC[CH-] ZPFKRQXYKULZKP-UHFFFAOYSA-N 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 235000011167 hydrochloric acid Nutrition 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- HITOXZPZGPXYHY-UJURSFKZSA-N levoglucosenone Chemical compound O=C1C=C[C@H]2CO[C@@H]1O2 HITOXZPZGPXYHY-UJURSFKZSA-N 0.000 description 1
- HITOXZPZGPXYHY-UHFFFAOYSA-N levoglucosenone Natural products O=C1C=CC2COC1O2 HITOXZPZGPXYHY-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/38—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D307/40—Radicals substituted by oxygen atoms
- C07D307/46—Doubly bound oxygen atoms, or two oxygen atoms singly bound to the same carbon atom
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Furan Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Vaporization, Distillation, Condensation, Sublimation, And Cold Traps (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP11193157 | 2011-12-13 | ||
| EP11193157.2 | 2011-12-13 | ||
| PCT/EP2012/075055 WO2013087613A1 (de) | 2011-12-13 | 2012-12-11 | Herstellung von 5-hydroxymethylfurfural (hmf) aus hexoselösungen in gegenwart von wasserdampf |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN104169263A CN104169263A (zh) | 2014-11-26 |
| CN104169263B true CN104169263B (zh) | 2016-06-15 |
Family
ID=47458896
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201280059056.3A Expired - Fee Related CN104169263B (zh) | 2011-12-13 | 2012-12-11 | 在蒸汽存在下由己糖溶液制备5-羟甲基糠醛(hmf) |
Country Status (10)
| Country | Link |
|---|---|
| EP (1) | EP2791126B1 (enExample) |
| JP (1) | JP6073363B2 (enExample) |
| KR (1) | KR101970853B1 (enExample) |
| CN (1) | CN104169263B (enExample) |
| BR (1) | BR112014014054B1 (enExample) |
| CA (1) | CA2856864C (enExample) |
| ES (1) | ES2626835T3 (enExample) |
| HU (1) | HUE033363T2 (enExample) |
| RU (1) | RU2014128460A (enExample) |
| WO (1) | WO2013087613A1 (enExample) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9156802B2 (en) | 2011-12-13 | 2015-10-13 | Basf Se | Separating off 5-hydroxymethylfurfural (HMF) from reaction solutions by steam distillation |
| DE102016224073A1 (de) * | 2016-12-02 | 2018-06-07 | Südzucker AG | Verbessertes HMF-Herstellungsverfahren |
| CN113825745B (zh) * | 2019-04-15 | 2025-04-04 | 斯道拉恩索公司 | 用于回收溶剂和分离腐殖质材料及其组合物的方法 |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2929823A (en) * | 1956-11-26 | 1960-03-22 | Merck & Co Inc | Production of 5-hydroxymethylfurfural |
| US3201331A (en) * | 1962-10-17 | 1965-08-17 | Atlas Chem Ind | Purification of hydroxymethyl furfural |
| FR2663933A1 (fr) * | 1990-06-27 | 1992-01-03 | Beghin Say Sa | Nouveau procede de preparation du 5-hydroxymethylfurfural a partir de saccharides. |
| CN101456850A (zh) * | 2007-12-12 | 2009-06-17 | 中国科学院大连化学物理研究所 | 一种制备5-羟甲基糠醛的方法 |
| CN101812039A (zh) * | 2010-05-14 | 2010-08-25 | 天津大学 | 一种利用离子液体催化生成5-羟甲基糠醛的方法 |
| CN102399203A (zh) * | 2011-12-19 | 2012-04-04 | 浙江大学 | 一种离子液体降解碳水化合物制备5-羟甲基糠醛的方法 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3601281A1 (de) | 1986-01-17 | 1987-07-23 | Sueddeutsche Zucker Ag | Verfahren zur herstellung von 5-hydroxymethylfurfural einschliesslich eines kristallinen produktes unter ausschliesslicher verwendung von wasser als loesungsmittel |
| EP1834950A1 (en) | 2006-03-10 | 2007-09-19 | Avantium International B.V. | Method for the synthesis of 5-alkoxymethylfurfural ethers and their use |
| EP1834951A1 (en) | 2006-03-10 | 2007-09-19 | Avantium International B.V. | Method for the synthesis of organic acid esters of 5-hydroxymethylfurfural and their use |
| EP2033958A1 (en) * | 2007-09-07 | 2009-03-11 | Furanix Technologies B.V | Hydroxymethylfurfural ethers from sugars and di- and triols |
-
2012
- 2012-12-11 CA CA2856864A patent/CA2856864C/en not_active Expired - Fee Related
- 2012-12-11 BR BR112014014054-5A patent/BR112014014054B1/pt not_active IP Right Cessation
- 2012-12-11 ES ES12808306.0T patent/ES2626835T3/es active Active
- 2012-12-11 KR KR1020147019046A patent/KR101970853B1/ko not_active Expired - Fee Related
- 2012-12-11 HU HUE12808306A patent/HUE033363T2/en unknown
- 2012-12-11 WO PCT/EP2012/075055 patent/WO2013087613A1/de not_active Ceased
- 2012-12-11 RU RU2014128460A patent/RU2014128460A/ru not_active Application Discontinuation
- 2012-12-11 EP EP12808306.0A patent/EP2791126B1/de not_active Not-in-force
- 2012-12-11 JP JP2014546456A patent/JP6073363B2/ja not_active Expired - Fee Related
- 2012-12-11 CN CN201280059056.3A patent/CN104169263B/zh not_active Expired - Fee Related
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2929823A (en) * | 1956-11-26 | 1960-03-22 | Merck & Co Inc | Production of 5-hydroxymethylfurfural |
| US3201331A (en) * | 1962-10-17 | 1965-08-17 | Atlas Chem Ind | Purification of hydroxymethyl furfural |
| FR2663933A1 (fr) * | 1990-06-27 | 1992-01-03 | Beghin Say Sa | Nouveau procede de preparation du 5-hydroxymethylfurfural a partir de saccharides. |
| CN101456850A (zh) * | 2007-12-12 | 2009-06-17 | 中国科学院大连化学物理研究所 | 一种制备5-羟甲基糠醛的方法 |
| CN101812039A (zh) * | 2010-05-14 | 2010-08-25 | 天津大学 | 一种利用离子液体催化生成5-羟甲基糠醛的方法 |
| CN102399203A (zh) * | 2011-12-19 | 2012-04-04 | 浙江大学 | 一种离子液体降解碳水化合物制备5-羟甲基糠醛的方法 |
Non-Patent Citations (7)
| Title |
|---|
| 5-Hydroxymethylfurfural (HMF) as a building block platform: Biological properties, synthesis and synthetic applications;Andreia A. Rosatella et al.;《Green Chemistry》;20110228;第13卷;第754-793页 * |
| 5-Hydroxymethylfurfural (HMF). A Review Focussing on its Manufacture;B. F. M. Kuster et al.;《Starch/starke》;19901231;第42卷;第314-321页 * |
| Catalytic pyrolysis of cellulose in sulfolane with some acidic catalysts;Haruo Kawamoto et al.;《J. Wood Sci.》;20061202;第53卷;第127-133页 * |
| Production of 5-hydroxymethylfurfural and furfural by dehydration of biomass-derived mono- and poly-saccharides;Juben N. Chheda et al.;《Green Chemistry》;20070117;第9卷;第342-350页 * |
| The Conversion of Fructose and Glucose in Acidic Media: Formation of Hydroxymethylfurfural;H. E. van Dam et al.;《Starch/starke》;19861231;第38卷;第95-101页 * |
| 水蒸气蒸馏技术在精细化学品生产中的应用;张珍明;《化工时刊》;20040625;第18卷(第6期);第48-49页 * |
| 薄膜蒸发器的应用;尹侠等;《化工设备与防腐蚀》;20020620;第5卷(第3期);第188-189页 * |
Also Published As
| Publication number | Publication date |
|---|---|
| EP2791126A1 (de) | 2014-10-22 |
| CA2856864A1 (en) | 2013-06-20 |
| CA2856864C (en) | 2021-05-25 |
| BR112014014054B1 (pt) | 2019-03-19 |
| RU2014128460A (ru) | 2016-02-10 |
| EP2791126B1 (de) | 2017-03-01 |
| HUE033363T2 (en) | 2017-11-28 |
| WO2013087613A1 (de) | 2013-06-20 |
| KR20140101849A (ko) | 2014-08-20 |
| JP2015500313A (ja) | 2015-01-05 |
| CN104169263A (zh) | 2014-11-26 |
| JP6073363B2 (ja) | 2017-02-01 |
| KR101970853B1 (ko) | 2019-04-19 |
| BR112014014054A2 (pt) | 2017-06-13 |
| ES2626835T3 (es) | 2017-07-26 |
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| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| CF01 | Termination of patent right due to non-payment of annual fee | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20160615 |