JP2017537096A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2017537096A5 JP2017537096A5 JP2017528450A JP2017528450A JP2017537096A5 JP 2017537096 A5 JP2017537096 A5 JP 2017537096A5 JP 2017528450 A JP2017528450 A JP 2017528450A JP 2017528450 A JP2017528450 A JP 2017528450A JP 2017537096 A5 JP2017537096 A5 JP 2017537096A5
- Authority
- JP
- Japan
- Prior art keywords
- water
- volume
- yield
- mvg
- solvent
- 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.)
- Granted
Links
- JBKTVPSFVUFSAO-UHFFFAOYSA-N methyl 2-hydroxybut-3-enoate Chemical compound COC(=O)C(O)C=C JBKTVPSFVUFSAO-UHFFFAOYSA-N 0.000 description 27
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 21
- WGCNASOHLSPBMP-UHFFFAOYSA-N Glycolaldehyde Chemical compound OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 16
- 239000002904 solvent Substances 0.000 description 13
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
- 238000000034 method Methods 0.000 description 8
- 239000003960 organic solvent Substances 0.000 description 6
- NYPNCQTUZYWFGG-UHFFFAOYSA-N 2,2-dimethoxyethanol Chemical compound COC(CO)OC NYPNCQTUZYWFGG-UHFFFAOYSA-N 0.000 description 4
- LPEKGGXMPWTOCB-UHFFFAOYSA-N 8beta-(2,3-epoxy-2-methylbutyryloxy)-14-acetoxytithifolin Natural products COC(=O)C(C)O LPEKGGXMPWTOCB-UHFFFAOYSA-N 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- ODQWQRRAPPTVAG-GZTJUZNOSA-N doxepin Chemical compound C1OC2=CC=CC=C2C(=C/CCN(C)C)/C2=CC=CC=C21 ODQWQRRAPPTVAG-GZTJUZNOSA-N 0.000 description 4
- 239000011968 lewis acid catalyst Substances 0.000 description 4
- 229940057867 methyl lactate Drugs 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 229910021536 Zeolite Inorganic materials 0.000 description 3
- -1 alkali metal salt Chemical class 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 238000005112 continuous flow technique Methods 0.000 description 3
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 3
- 239000010457 zeolite Substances 0.000 description 3
- 229930091371 Fructose Natural products 0.000 description 2
- 239000005715 Fructose Substances 0.000 description 2
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 description 2
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 229960004016 sucrose syrup Drugs 0.000 description 2
- NEEIJIVVRBIWKC-UHFFFAOYSA-N 2-hydroxy-2-methylpropanoic acid;2-hydroxypropanoic acid Chemical compound CC(O)C(O)=O.CC(C)(O)C(O)=O NEEIJIVVRBIWKC-UHFFFAOYSA-N 0.000 description 1
- VBWPSWWDYVWZKA-UHFFFAOYSA-N 2-hydroxybut-3-enoic acid Chemical compound C=CC(O)C(O)=O VBWPSWWDYVWZKA-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229930006000 Sucrose Natural products 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
- 150000001299 aldehydes Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000001360 methionine group Chemical class N[C@@H](CCSC)C(=O)* 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 235000020374 simple syrup Nutrition 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229960004793 sucrose Drugs 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP14195485 | 2014-11-28 | ||
| EP14195485.9 | 2014-11-28 | ||
| DKPA201500288 | 2015-05-13 | ||
| DKPA201500288 | 2015-05-13 | ||
| PCT/EP2015/076399 WO2016083137A1 (en) | 2014-11-28 | 2015-11-12 | Process for preparing esters of lactic acid, and 2-hydroxy-3-butenoic acid or alfa-hydroxy methionine analogues from sugars |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2020070960A Division JP6826225B2 (ja) | 2014-11-28 | 2020-04-10 | 糖から乳酸及び２−ヒドロキシ−３−ブテン酸又はα−ヒドロキシメチオニン類似体のエステルを製造する方法 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2017537096A JP2017537096A (ja) | 2017-12-14 |
| JP2017537096A5 true JP2017537096A5 (enExample) | 2019-02-14 |
| JP6788588B2 JP6788588B2 (ja) | 2020-11-25 |
Family
ID=59019550
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017528450A Active JP6788588B2 (ja) | 2014-11-28 | 2015-11-12 | 糖から乳酸及び２−ヒドロキシ−３−ブテン酸又はα−ヒドロキシメチオニン類似体のエステルを製造する方法 |
| JP2020070960A Expired - Fee Related JP6826225B2 (ja) | 2014-11-28 | 2020-04-10 | 糖から乳酸及び２−ヒドロキシ−３−ブテン酸又はα−ヒドロキシメチオニン類似体のエステルを製造する方法 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2020070960A Expired - Fee Related JP6826225B2 (ja) | 2014-11-28 | 2020-04-10 | 糖から乳酸及び２−ヒドロキシ−３−ブテン酸又はα−ヒドロキシメチオニン類似体のエステルを製造する方法 |
Country Status (19)
| Country | Link |
|---|---|
| US (3) | US10100007B2 (enExample) |
| EP (2) | EP3224234B1 (enExample) |
| JP (2) | JP6788588B2 (enExample) |
| KR (1) | KR102475064B1 (enExample) |
| CN (2) | CN109942466B (enExample) |
| AU (1) | AU2015352840B2 (enExample) |
| BR (1) | BR112017011304B1 (enExample) |
| CA (1) | CA2968906C (enExample) |
| CU (1) | CU24499B1 (enExample) |
| DK (2) | DK3461806T3 (enExample) |
| ES (2) | ES2813341T3 (enExample) |
| HU (2) | HUE046852T2 (enExample) |
| MX (2) | MX2017006538A (enExample) |
| MY (1) | MY194486A (enExample) |
| PL (2) | PL3224234T3 (enExample) |
| RU (2) | RU2710014C2 (enExample) |
| SG (2) | SG11201704329UA (enExample) |
| WO (1) | WO2016083137A1 (enExample) |
| ZA (1) | ZA201703204B (enExample) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3224234B1 (en) | 2014-11-28 | 2019-08-14 | Haldor Topsøe A/S | Process for preparing esters of lactic acid and 2-hydroxy-3-butenoic acid from sugars |
| TWI713520B (zh) | 2015-04-30 | 2020-12-21 | 丹麥商托普索公司 | 從糖類及其衍生物製備甲硫胺酸α-羥基類似物的方法 |
| TWI712584B (zh) | 2016-05-04 | 2020-12-11 | 丹麥商托普索公司 | 新穎己二酯類化合物及其製備方法 |
| CN106349060B (zh) * | 2016-08-26 | 2020-06-12 | 上海交通大学 | 一种路易斯酸催化转化碳水化合物制备乳酸烷基酯的方法 |
| CN109289909B (zh) * | 2018-10-16 | 2021-03-19 | 郑州大学 | 一种催化复杂糖转化制备乳酸酯的催化剂 |
| CN114341107A (zh) * | 2019-09-06 | 2022-04-12 | 建明实业股份有限公司 | 通过酯化α-羟基酸制备α-羟基酯的工艺 |
| CN111905802B (zh) * | 2020-06-15 | 2022-01-18 | 厦门大学 | 一种使用钼-碱金属/碱土金属修饰的路易斯酸催化剂制乳酸酯的方法 |
| CN113831238B (zh) * | 2020-06-24 | 2024-05-03 | 中国石油化工股份有限公司 | 一种催化转化碳水化合物制备乳酸甲酯的方法 |
| CN116272945B (zh) * | 2023-01-16 | 2024-12-31 | 山东理工大学 | 酸碱碳基催化剂的制备方法及应用 |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4792620A (en) * | 1983-10-14 | 1988-12-20 | Bp Chemicals Limited | Carbonylation catalysts |
| US4933161A (en) | 1987-02-04 | 1990-06-12 | Exxon Research And Engineering Company | Tin substitution into zeolite frameworks |
| US5973200A (en) * | 1997-01-23 | 1999-10-26 | Novus International, Inc. | Process for the preparation of 2-hydroxy-4-(methylthio) butanoic acid or methionine by mercaptan addition |
| DE10140202A1 (de) | 2001-08-16 | 2003-03-06 | Bayer Ag | Vanadium-Imido-Phosphoraniminato für die Olefinpolymerisation |
| DE102005003990A1 (de) * | 2005-01-28 | 2006-08-03 | Degussa Ag | Herstellung von 3-(Alkylthio)propanal |
| ES2401537T3 (es) * | 2008-11-11 | 2013-04-22 | Haldor Topsoe A/S | Preparación catalizada por zeolita de compuestos de ácidos alfa-hidroxicarboxílicos y ésteres de los mismos |
| FR2938535B1 (fr) * | 2008-11-20 | 2012-08-17 | Arkema France | Procede de fabrication de methylmercaptopropionaldehyde et de methionine a partir de matieres renouvelables |
| ES2667496T3 (es) * | 2009-04-03 | 2018-05-11 | Mitsubishi Gas Chemical Company, Inc. | Método para producir éster del ácido alfa-hidroxicarboxílico |
| TWI630197B (zh) | 2013-02-27 | 2018-07-21 | 丹麥商哈爾德杜薩公司 | 從包含低分子量羰基化合物之組成物移除甲醛的方法 |
| ES2657987T3 (es) | 2013-08-20 | 2018-03-07 | Haldor Topsoe A/S | Procedimiento para la conversión de azúcares en ácido láctico y ácido 2-hidroxi-3-butenoico o sus ésteres que comprenden un material de metalo-silicato y un ion de metal |
| EP3224234B1 (en) | 2014-11-28 | 2019-08-14 | Haldor Topsøe A/S | Process for preparing esters of lactic acid and 2-hydroxy-3-butenoic acid from sugars |
-
2015
- 2015-11-12 EP EP15793830.9A patent/EP3224234B1/en active Active
- 2015-11-12 CU CU2017000072A patent/CU24499B1/es unknown
- 2015-11-12 CN CN201910108607.4A patent/CN109942466B/zh not_active Expired - Fee Related
- 2015-11-12 US US15/525,450 patent/US10100007B2/en not_active Expired - Fee Related
- 2015-11-12 PL PL15793830T patent/PL3224234T3/pl unknown
- 2015-11-12 SG SG11201704329UA patent/SG11201704329UA/en unknown
- 2015-11-12 ES ES18204431T patent/ES2813341T3/es active Active
- 2015-11-12 WO PCT/EP2015/076399 patent/WO2016083137A1/en not_active Ceased
- 2015-11-12 PL PL18204431T patent/PL3461806T3/pl unknown
- 2015-11-12 MX MX2017006538A patent/MX2017006538A/es unknown
- 2015-11-12 CA CA2968906A patent/CA2968906C/en active Active
- 2015-11-12 MY MYPI2020003140A patent/MY194486A/en unknown
- 2015-11-12 HU HUE15793830A patent/HUE046852T2/hu unknown
- 2015-11-12 ES ES15793830T patent/ES2748690T3/es active Active
- 2015-11-12 AU AU2015352840A patent/AU2015352840B2/en active Active
- 2015-11-12 SG SG10201810447YA patent/SG10201810447YA/en unknown
- 2015-11-12 RU RU2017122603A patent/RU2710014C2/ru active
- 2015-11-12 RU RU2019131408A patent/RU2019131408A/ru unknown
- 2015-11-12 JP JP2017528450A patent/JP6788588B2/ja active Active
- 2015-11-12 DK DK18204431.3T patent/DK3461806T3/da active
- 2015-11-12 BR BR112017011304A patent/BR112017011304B1/pt active IP Right Grant
- 2015-11-12 CN CN201580065008.9A patent/CN107001253B/zh active Active
- 2015-11-12 EP EP18204431.3A patent/EP3461806B1/en active Active
- 2015-11-12 KR KR1020177015149A patent/KR102475064B1/ko active Active
- 2015-11-12 HU HUE18204431A patent/HUE051552T2/hu unknown
- 2015-11-12 DK DK15793830T patent/DK3224234T3/da active
-
2017
- 2017-05-09 ZA ZA201703204A patent/ZA201703204B/en unknown
- 2017-05-18 MX MX2020011677A patent/MX2020011677A/es unknown
-
2018
- 2018-09-17 US US16/133,146 patent/US10343986B2/en active Active
- 2018-09-17 US US16/133,100 patent/US10280136B2/en active Active
-
2020
- 2020-04-10 JP JP2020070960A patent/JP6826225B2/ja not_active Expired - Fee Related
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP6826225B2 (ja) | 糖から乳酸及び２−ヒドロキシ−３−ブテン酸又はα−ヒドロキシメチオニン類似体のエステルを製造する方法 | |
| JP6431913B2 (ja) | メタロシリケート材料及び金属イオンを含む乳酸及び２−ヒドロキシ−３−ブテン酸又はそれらのエステルの糖への転化方法 | |
| He et al. | Catalytic Upgrading of Biomass‐Derived Sugars with Acidic Nanoporous Materials: Structural Role in Carbon‐Chain Length Variation | |
| BRPI0904364B1 (pt) | processo para a produção de ácido láctico e ácido 2-hidróxi-3-butenóico ou ésteres dos mesmos | |
| FR3071498B1 (fr) | Procede de production de 5-hydroxymethylfurfural en presence d'un catalyseur de deshydratation organique et d'une source de chlorure | |
| JP2016536324A5 (enExample) | ||
| WO2015127662A1 (en) | Synthesis of diketone compounds from carbohydrates | |
| CN104292214A (zh) | 艾氟康唑及其中间体的合成方法 | |
| CN108794435A (zh) | 一种用于生物质糠醛类化合物在乙醇中的整合催化转化方法 | |
| JP2017525662A5 (enExample) | ||
| JP6908529B2 (ja) | 糖およびその誘導体からのメチオニンα−ヒドロキシ類似体の製造方法 | |
| CN103827074A (zh) | 由内酯生产烯酸酯的方法 | |
| CN107787313B (zh) | 由c6和c5糖制备2,5,6-三羟基-3-己烯酸和2,5-二羟基-3-戊烯酸及其酯 | |
| TWI791754B (zh) | α-羥基化合物的製造方法及其用途 | |
| BR122018073240B1 (pt) | Processo de fluxo contínuo para a preparação de um a-hidróxianálogo da metionina | |
| HK1234387B (zh) | 由糖制备乳酸酯和2-羟基-3-丁烯酸酯或α-羟基蛋氨酸类似物的酯的方法 | |
| EP3106452A1 (en) | Preparation of 2,5,6-trihydroxy-3-hexenoic acid and 2,5-dihydroxy-3-pentenoic acid and esters thereof from c6 and c5 sugars |