IL192619A - Method for preparing 3-hydroxytetrahydrofuran using cyclodehydration - Google Patents
Method for preparing 3-hydroxytetrahydrofuran using cyclodehydrationInfo
- Publication number
- IL192619A IL192619A IL192619A IL19261908A IL192619A IL 192619 A IL192619 A IL 192619A IL 192619 A IL192619 A IL 192619A IL 19261908 A IL19261908 A IL 19261908A IL 192619 A IL192619 A IL 192619A
- Authority
- IL
- Israel
- Prior art keywords
- cyclodehydration
- hydroxytetrahydrofuran
- reaction
- preparing
- butanetriol
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 24
- 238000006210 cyclodehydration reaction Methods 0.000 title claims description 21
- XDPCNPCKDGQBAN-UHFFFAOYSA-N 3-hydroxytetrahydrofuran Chemical compound OC1CCOC1 XDPCNPCKDGQBAN-UHFFFAOYSA-N 0.000 title claims description 19
- 238000006243 chemical reaction Methods 0.000 claims description 32
- ARXKVVRQIIOZGF-UHFFFAOYSA-N 1,2,4-butanetriol Chemical compound OCCC(O)CO ARXKVVRQIIOZGF-UHFFFAOYSA-N 0.000 claims description 24
- 239000003054 catalyst Substances 0.000 claims description 16
- 239000002253 acid Substances 0.000 claims description 11
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 claims description 10
- 239000000376 reactant Substances 0.000 claims description 10
- 125000000542 sulfonic acid group Chemical group 0.000 claims description 8
- 239000003456 ion exchange resin Substances 0.000 claims description 6
- 229920003303 ion-exchange polymer Polymers 0.000 claims description 6
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 claims description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 4
- 239000003729 cation exchange resin Substances 0.000 claims description 4
- 229920001577 copolymer Polymers 0.000 claims description 2
- 229910006069 SO3H Inorganic materials 0.000 claims 1
- 230000003287 optical effect Effects 0.000 description 16
- 238000002360 preparation method Methods 0.000 description 7
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- ARXKVVRQIIOZGF-BYPYZUCNSA-N 2-deoxyerythritol Chemical compound OCC[C@H](O)CO ARXKVVRQIIOZGF-BYPYZUCNSA-N 0.000 description 3
- 229910000619 316 stainless steel Inorganic materials 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- 239000002202 Polyethylene glycol Substances 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000007796 conventional method Methods 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 229920001223 polyethylene glycol Polymers 0.000 description 3
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 3
- ARXKVVRQIIOZGF-SCSAIBSYSA-N (2r)-butane-1,2,4-triol Chemical compound OCC[C@@H](O)CO ARXKVVRQIIOZGF-SCSAIBSYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 229920002565 Polyethylene Glycol 400 Polymers 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- GTTSNKDQDACYLV-UHFFFAOYSA-N Trihydroxybutane Chemical compound CCCC(O)(O)O GTTSNKDQDACYLV-UHFFFAOYSA-N 0.000 description 2
- 238000010924 continuous production Methods 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 2
- -1 ether Chemical compound 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 150000007522 mineralic acids Chemical class 0.000 description 2
- 239000002798 polar solvent Substances 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- XDPCNPCKDGQBAN-SCSAIBSYSA-N (3r)-oxolan-3-ol Chemical compound O[C@@H]1CCOC1 XDPCNPCKDGQBAN-SCSAIBSYSA-N 0.000 description 1
- XDPCNPCKDGQBAN-BYPYZUCNSA-N (3s)-oxolan-3-ol Chemical compound O[C@H]1CCOC1 XDPCNPCKDGQBAN-BYPYZUCNSA-N 0.000 description 1
- YZUPZGFPHUVJKC-UHFFFAOYSA-N 1-bromo-2-methoxyethane Chemical compound COCCBr YZUPZGFPHUVJKC-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000003377 acid catalyst Substances 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 239000003905 agrochemical Substances 0.000 description 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 1
- 238000010960 commercial process Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000006340 racemization Effects 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000008096 xylene Substances 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
- C07D307/04—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D307/18—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D307/20—Oxygen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Furan Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/KR2006/000091 WO2007081065A1 (en) | 2006-01-10 | 2006-01-10 | Method for preparing 3-hydroxytetrahydrofuran using cyclodehydration |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IL192619A0 IL192619A0 (en) | 2009-02-11 |
| IL192619A true IL192619A (en) | 2013-03-24 |
Family
ID=38256458
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL192619A IL192619A (en) | 2006-01-10 | 2008-07-03 | Method for preparing 3-hydroxytetrahydrofuran using cyclodehydration |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US8124796B2 (enExample) |
| EP (1) | EP1971589B1 (enExample) |
| JP (1) | JP5083670B2 (enExample) |
| CN (1) | CN101356166B (enExample) |
| ES (1) | ES2444570T3 (enExample) |
| IL (1) | IL192619A (enExample) |
| WO (1) | WO2007081065A1 (enExample) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5177759B2 (ja) * | 2008-03-26 | 2013-04-10 | 独立行政法人産業技術総合研究所 | 多価アルコールからの環状エーテル及びヒドロキシケトンの製造方法 |
| CN102071231B (zh) * | 2010-11-30 | 2012-12-12 | 浙江工业大学 | 一种微生物转化制备s-(+)-3-羟基四氢呋喃的方法 |
| CN103044365B (zh) * | 2011-10-17 | 2015-06-17 | 中国石油化工股份有限公司 | 一种四氢呋喃的生产方法 |
| US9600312B2 (en) | 2014-09-30 | 2017-03-21 | Amazon Technologies, Inc. | Threading as a service |
| US9588790B1 (en) | 2015-02-04 | 2017-03-07 | Amazon Technologies, Inc. | Stateful virtual compute system |
| CN104961711B (zh) * | 2015-07-23 | 2017-03-08 | 沧州那瑞化学科技有限公司 | （s）‑3‑羟基四氢呋喃和（r）‑3‑羟基四氢呋喃的制备方法 |
| DE102017008071A1 (de) * | 2017-08-28 | 2019-02-28 | Henkel Ag & Co. Kgaa | Neue anionische Tenside und Wasch- und Reinigungsmittel, welche diese enthalten |
| CN108620103B (zh) * | 2018-04-23 | 2021-07-06 | 南京工业大学 | 一种制备(s)-3-羟基四氢呋喃的催化剂及其制备与使用方法 |
| US11119809B1 (en) | 2019-06-20 | 2021-09-14 | Amazon Technologies, Inc. | Virtualization-based transaction handling in an on-demand network code execution system |
| CN110618208A (zh) * | 2019-09-10 | 2019-12-27 | 威海迪素制药有限公司 | 一种（s）-（+）-3-羟基四氢呋喃对映异构体含量检测方法 |
| US11263220B2 (en) | 2019-09-27 | 2022-03-01 | Amazon Technologies, Inc. | On-demand execution of object transformation code in output path of object storage service |
| US11360948B2 (en) | 2019-09-27 | 2022-06-14 | Amazon Technologies, Inc. | Inserting owner-specified data processing pipelines into input/output path of object storage service |
| US11394761B1 (en) | 2019-09-27 | 2022-07-19 | Amazon Technologies, Inc. | Execution of user-submitted code on a stream of data |
| US11714682B1 (en) | 2020-03-03 | 2023-08-01 | Amazon Technologies, Inc. | Reclaiming computing resources in an on-demand code execution system |
| US11775640B1 (en) | 2020-03-30 | 2023-10-03 | Amazon Technologies, Inc. | Resource utilization-based malicious task detection in an on-demand code execution system |
| US11550713B1 (en) | 2020-11-25 | 2023-01-10 | Amazon Technologies, Inc. | Garbage collection in distributed systems using life cycled storage roots |
| US11593270B1 (en) | 2020-11-25 | 2023-02-28 | Amazon Technologies, Inc. | Fast distributed caching using erasure coded object parts |
| CN114195743A (zh) * | 2021-12-02 | 2022-03-18 | 厦门弘毅元素科技有限公司 | 一种（s）-3-羟基四氢呋喃的合成方法 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3308931A1 (de) * | 1983-03-12 | 1984-09-20 | Basf Ag, 6700 Ludwigshafen | Verfahren zur herstellung von 3-hydroxytetrahydrofuran |
| JP3855033B2 (ja) * | 1995-09-08 | 2006-12-06 | 高砂香料工業株式会社 | 光学活性３−ヒドロキシ−γ−ブチロラクトンの製造方法 |
| JP4503754B2 (ja) * | 1999-04-15 | 2010-07-14 | 株式会社カネカ | ３−ヒドロキシテトラヒドロフランの製造方法 |
-
2006
- 2006-01-10 US US12/160,261 patent/US8124796B2/en active Active
- 2006-01-10 CN CN2006800505230A patent/CN101356166B/zh not_active Expired - Fee Related
- 2006-01-10 EP EP06700116.4A patent/EP1971589B1/en not_active Not-in-force
- 2006-01-10 JP JP2008549400A patent/JP5083670B2/ja not_active Expired - Fee Related
- 2006-01-10 WO PCT/KR2006/000091 patent/WO2007081065A1/en not_active Ceased
- 2006-01-10 ES ES06700116.4T patent/ES2444570T3/es active Active
-
2008
- 2008-07-03 IL IL192619A patent/IL192619A/en active IP Right Grant
Also Published As
| Publication number | Publication date |
|---|---|
| US8124796B2 (en) | 2012-02-28 |
| WO2007081065A1 (en) | 2007-07-19 |
| JP5083670B2 (ja) | 2012-11-28 |
| CN101356166B (zh) | 2012-05-23 |
| EP1971589A1 (en) | 2008-09-24 |
| EP1971589B1 (en) | 2013-11-06 |
| US20090005581A1 (en) | 2009-01-01 |
| CN101356166A (zh) | 2009-01-28 |
| EP1971589A4 (en) | 2010-12-22 |
| ES2444570T3 (es) | 2014-02-25 |
| JP2009522350A (ja) | 2009-06-11 |
| IL192619A0 (en) | 2009-02-11 |
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Legal Events
| Date | Code | Title | Description |
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| FF | Patent granted | ||
| KB | Patent renewed | ||
| KB | Patent renewed |