CN104961711A - (s)-3-羟基四氢呋喃和(r)-3-羟基四氢呋喃的制备方法 - Google Patents
(s)-3-羟基四氢呋喃和(r)-3-羟基四氢呋喃的制备方法 Download PDFInfo
- Publication number
- CN104961711A CN104961711A CN201510436829.0A CN201510436829A CN104961711A CN 104961711 A CN104961711 A CN 104961711A CN 201510436829 A CN201510436829 A CN 201510436829A CN 104961711 A CN104961711 A CN 104961711A
- Authority
- CN
- China
- Prior art keywords
- dihydroxyl
- trimethylammonium
- preparation
- hydroxyl tetrahydrofuran
- reaction
- 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
- 238000002360 preparation method Methods 0.000 title claims abstract description 53
- XDPCNPCKDGQBAN-BYPYZUCNSA-N (3s)-oxolan-3-ol Chemical compound O[C@H]1CCOC1 XDPCNPCKDGQBAN-BYPYZUCNSA-N 0.000 title claims abstract description 33
- XDPCNPCKDGQBAN-SCSAIBSYSA-N (3r)-oxolan-3-ol Chemical compound O[C@@H]1CCOC1 XDPCNPCKDGQBAN-SCSAIBSYSA-N 0.000 title claims abstract description 19
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 105
- 238000006243 chemical reaction Methods 0.000 claims abstract description 69
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 claims abstract description 62
- 239000003513 alkali Substances 0.000 claims abstract description 40
- DDUHZTYCFQRHIY-UHFFFAOYSA-N 7-chloro-3',4,6-trimethoxy-5'-methylspiro[1-benzofuran-2,4'-cyclohex-2-ene]-1',3-dione Chemical compound COC1=CC(=O)CC(C)C11C(=O)C(C(OC)=CC(OC)=C2Cl)=C2O1 DDUHZTYCFQRHIY-UHFFFAOYSA-N 0.000 claims abstract description 36
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims abstract description 26
- 229910000041 hydrogen chloride Inorganic materials 0.000 claims abstract description 26
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 claims abstract description 26
- 239000003960 organic solvent Substances 0.000 claims abstract description 21
- PHIQHXFUZVPYII-LURJTMIESA-N (S)-carnitine Chemical compound C[N+](C)(C)C[C@@H](O)CC([O-])=O PHIQHXFUZVPYII-LURJTMIESA-N 0.000 claims abstract description 17
- PHIQHXFUZVPYII-ZCFIWIBFSA-N (R)-carnitine Chemical compound C[N+](C)(C)C[C@H](O)CC([O-])=O PHIQHXFUZVPYII-ZCFIWIBFSA-N 0.000 claims abstract description 12
- 239000002994 raw material Substances 0.000 claims abstract description 12
- 229960001518 levocarnitine Drugs 0.000 claims abstract description 10
- 239000002798 polar solvent Substances 0.000 claims abstract description 5
- 238000006722 reduction reaction Methods 0.000 claims abstract description 5
- 238000007363 ring formation reaction Methods 0.000 claims abstract description 4
- 238000010438 heat treatment Methods 0.000 claims abstract description 3
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical group C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 84
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical group CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 75
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 44
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N dimethyl sulfoxide Natural products CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims description 42
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 30
- 230000002829 reductive effect Effects 0.000 claims description 28
- 239000012279 sodium borohydride Substances 0.000 claims description 11
- 229910000033 sodium borohydride Inorganic materials 0.000 claims description 11
- 239000003795 chemical substances by application Substances 0.000 claims description 10
- JMMWKPVZQRWMSS-UHFFFAOYSA-N isopropanol acetate Natural products CC(C)OC(C)=O JMMWKPVZQRWMSS-UHFFFAOYSA-N 0.000 claims description 10
- 229940011051 isopropyl acetate Drugs 0.000 claims description 10
- GWYFCOCPABKNJV-UHFFFAOYSA-N isovaleric acid Chemical compound CC(C)CC(O)=O GWYFCOCPABKNJV-UHFFFAOYSA-N 0.000 claims description 10
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 9
- 239000012321 sodium triacetoxyborohydride Substances 0.000 claims description 3
- 238000000034 method Methods 0.000 abstract description 9
- 150000002391 heterocyclic compounds Chemical class 0.000 abstract description 2
- 239000003638 chemical reducing agent Substances 0.000 abstract 1
- 238000009776 industrial production Methods 0.000 abstract 1
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 1
- 238000003756 stirring Methods 0.000 description 36
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 27
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 18
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 18
- 238000001816 cooling Methods 0.000 description 18
- 239000000706 filtrate Substances 0.000 description 18
- 238000000967 suction filtration Methods 0.000 description 18
- 238000005406 washing Methods 0.000 description 18
- 239000000047 product Substances 0.000 description 12
- 239000000126 substance Substances 0.000 description 10
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 9
- 239000012043 crude product Substances 0.000 description 9
- 239000000284 extract Substances 0.000 description 9
- 239000005457 ice water Substances 0.000 description 9
- 238000002156 mixing Methods 0.000 description 9
- 230000003287 optical effect Effects 0.000 description 9
- 239000012074 organic phase Substances 0.000 description 9
- 238000011084 recovery Methods 0.000 description 9
- 150000003839 salts Chemical class 0.000 description 9
- 239000002904 solvent Substances 0.000 description 9
- 238000010792 warming Methods 0.000 description 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- ARXKVVRQIIOZGF-UHFFFAOYSA-N 1,2,4-butanetriol Chemical compound OCCC(O)CO ARXKVVRQIIOZGF-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229960004203 carnitine Drugs 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 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
- 239000002699 waste material Substances 0.000 description 2
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 238000007033 dehydrochlorination reaction Methods 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 229940116298 l- malic acid Drugs 0.000 description 1
- OJURWUUOVGOHJZ-UHFFFAOYSA-N methyl 2-[(2-acetyloxyphenyl)methyl-[2-[(2-acetyloxyphenyl)methyl-(2-methoxy-2-oxoethyl)amino]ethyl]amino]acetate Chemical compound C=1C=CC=C(OC(C)=O)C=1CN(CC(=O)OC)CCN(CC(=O)OC)CC1=CC=CC=C1OC(C)=O OJURWUUOVGOHJZ-UHFFFAOYSA-N 0.000 description 1
- 238000006798 ring closing metathesis reaction Methods 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
- Cosmetics (AREA)
Abstract
Description
Claims (9)
Priority Applications (1)
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CN201510436829.0A CN104961711B (zh) | 2015-07-23 | 2015-07-23 | (s)‑3‑羟基四氢呋喃和(r)‑3‑羟基四氢呋喃的制备方法 |
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CN201510436829.0A CN104961711B (zh) | 2015-07-23 | 2015-07-23 | (s)‑3‑羟基四氢呋喃和(r)‑3‑羟基四氢呋喃的制备方法 |
Publications (2)
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CN104961711A true CN104961711A (zh) | 2015-10-07 |
CN104961711B CN104961711B (zh) | 2017-03-08 |
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113092629A (zh) * | 2021-04-14 | 2021-07-09 | 合肥利夫生物科技有限公司 | 一种s-(+)-3-羟基四氢呋喃的纯化和异构体检测方法 |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0765876A1 (en) * | 1995-09-29 | 1997-04-02 | Sigma-Tau Industrie Farmaceutiche Riunite S.p.A. | Process for the preparation of (s)-beta-hydroxy-gamma-butyrolactone |
WO2001047908A1 (en) * | 1999-12-23 | 2001-07-05 | Sigma-Tau Industrie Farmaceutiche Riunite S.P.A. | Stereospecific hydrolysis of optically active esters |
CN101356166A (zh) * | 2006-01-10 | 2009-01-28 | Sk株式会社 | 利用环化脱水作用制备3-羟基四氢呋喃的方法 |
CN102477019A (zh) * | 2010-11-26 | 2012-05-30 | 苏州凯达生物医药技术有限公司 | 制备s-3-羟基四氢呋喃的新方法 |
CN104478833A (zh) * | 2014-11-24 | 2015-04-01 | 苏州乔纳森新材料科技有限公司 | 一种(s)-(+)-3-羟基四氢呋喃的合成方法 |
CN104718196A (zh) * | 2012-11-13 | 2015-06-17 | 株式会社大赛璐 | 3-羟基四氢呋喃的制造方法、1,3-丁二醇的制造方法 |
-
2015
- 2015-07-23 CN CN201510436829.0A patent/CN104961711B/zh active Active
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0765876A1 (en) * | 1995-09-29 | 1997-04-02 | Sigma-Tau Industrie Farmaceutiche Riunite S.p.A. | Process for the preparation of (s)-beta-hydroxy-gamma-butyrolactone |
WO2001047908A1 (en) * | 1999-12-23 | 2001-07-05 | Sigma-Tau Industrie Farmaceutiche Riunite S.P.A. | Stereospecific hydrolysis of optically active esters |
CN101356166A (zh) * | 2006-01-10 | 2009-01-28 | Sk株式会社 | 利用环化脱水作用制备3-羟基四氢呋喃的方法 |
CN102477019A (zh) * | 2010-11-26 | 2012-05-30 | 苏州凯达生物医药技术有限公司 | 制备s-3-羟基四氢呋喃的新方法 |
CN104718196A (zh) * | 2012-11-13 | 2015-06-17 | 株式会社大赛璐 | 3-羟基四氢呋喃的制造方法、1,3-丁二醇的制造方法 |
CN104478833A (zh) * | 2014-11-24 | 2015-04-01 | 苏州乔纳森新材料科技有限公司 | 一种(s)-(+)-3-羟基四氢呋喃的合成方法 |
Non-Patent Citations (4)
Title |
---|
LUTZ GRAΒHOFF ET AL.: "Zur Stereochemie phenylsubstituierter Amiboalkanole", 《ARCH. PHARM.》 * |
STEPHEN LOWES ET AL.: "Simple and Unambiguous Method for Identifying Urinary Acylcarnitines Using Gas Chromatography - Mass Spectrometry", 《ANALYST》 * |
李勇智等: "手性化合物(S)-3-羟基四氢呋喃的合成", 《应用化工》 * |
王晓琴等: "药物中间体(S)-3-羟基四氢呋喃的合成研究", 《化学研究与应用》 * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113092629A (zh) * | 2021-04-14 | 2021-07-09 | 合肥利夫生物科技有限公司 | 一种s-(+)-3-羟基四氢呋喃的纯化和异构体检测方法 |
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CN104961711B (zh) | 2017-03-08 |
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PE01 | Entry into force of the registration of the contract for pledge of patent right |
Denomination of invention: Process for the preparation of (S) -3- hydroxy tetrahydrofuran and (R) -3- hydroxy tetrahydrofuran Effective date of registration: 20170418 Granted publication date: 20170308 Pledgee: Bank of Cangzhou Limited by Share Ltd. branch Pledgor: CANGZHOU SENARY CHEMICAL SCIENCE-TEC CO.,LTD. Registration number: 2017990000322 |
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Date of cancellation: 20190416 Granted publication date: 20170308 Pledgee: Bank of Cangzhou Limited by Share Ltd. branch Pledgor: CANGZHOU SENARY CHEMICAL SCIENCE-TEC CO.,LTD. Registration number: 2017990000322 |
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Denomination of invention: Process for the preparation of (S) -3- hydroxy tetrahydrofuran and (R) -3- hydroxy tetrahydrofuran Effective date of registration: 20190416 Granted publication date: 20170308 Pledgee: Bank of Cangzhou Limited by Share Ltd. branch Pledgor: CANGZHOU SENARY CHEMICAL SCIENCE-TEC CO.,LTD. Registration number: 2019990000327 |
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Date of cancellation: 20210414 Granted publication date: 20170308 Pledgee: Bank of Cangzhou Limited by Share Ltd. branch Pledgor: CANGZHOU SENARY CHEMICAL SCIENCE-TEC Co.,Ltd. Registration number: 2019990000327 |
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Denomination of invention: (S) Preparation of - 3-hydroxytetrahydrofuran and (R) - 3-hydroxytetrahydrofuran Effective date of registration: 20210414 Granted publication date: 20170308 Pledgee: Bank of Cangzhou Limited by Share Ltd. branch Pledgor: CANGZHOU SENARY CHEMICAL SCIENCE-TEC Co.,Ltd. Registration number: Y2021990000331 |
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