CN108299197A - 一种3-烷氧基丙烯酸酯合成方法 - Google Patents
一种3-烷氧基丙烯酸酯合成方法 Download PDFInfo
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- CN108299197A CN108299197A CN201810119820.0A CN201810119820A CN108299197A CN 108299197 A CN108299197 A CN 108299197A CN 201810119820 A CN201810119820 A CN 201810119820A CN 108299197 A CN108299197 A CN 108299197A
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- Prior art keywords
- acrylic esters
- added
- alkoxy acrylic
- synthetic method
- obtains
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Links
- 238000010189 synthetic method Methods 0.000 title claims abstract description 15
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims abstract description 36
- 125000001340 2-chloroethyl group Chemical class [H]C([H])(Cl)C([H])([H])* 0.000 claims abstract description 14
- -1 alkoxy acrylic ester Chemical class 0.000 claims abstract description 14
- 238000000034 method Methods 0.000 claims abstract description 12
- 150000002148 esters Chemical class 0.000 claims abstract description 9
- 239000002798 polar solvent Substances 0.000 claims abstract description 6
- 239000003054 catalyst Substances 0.000 claims abstract description 5
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 33
- 238000003756 stirring Methods 0.000 claims description 20
- 239000007788 liquid Substances 0.000 claims description 19
- 238000006243 chemical reaction Methods 0.000 claims description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- 238000010792 warming Methods 0.000 claims description 10
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical group CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims description 9
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 claims description 9
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims description 8
- 238000005194 fractionation Methods 0.000 claims description 8
- 239000012044 organic layer Substances 0.000 claims description 8
- 239000012074 organic phase Substances 0.000 claims description 8
- 238000013517 stratification Methods 0.000 claims description 7
- WBJINCZRORDGAQ-UHFFFAOYSA-N formic acid ethyl ester Natural products CCOC=O WBJINCZRORDGAQ-UHFFFAOYSA-N 0.000 claims description 5
- 239000010410 layer Substances 0.000 claims description 5
- 239000000725 suspension Substances 0.000 claims description 5
- 238000005406 washing Methods 0.000 claims description 5
- 238000010438 heat treatment Methods 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 239000003112 inhibitor Substances 0.000 claims description 4
- TZIHFWKZFHZASV-UHFFFAOYSA-N methyl formate Chemical compound COC=O TZIHFWKZFHZASV-UHFFFAOYSA-N 0.000 claims description 4
- 238000006116 polymerization reaction Methods 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 claims description 3
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 3
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 claims description 3
- 238000013019 agitation Methods 0.000 claims description 2
- 239000012046 mixed solvent Substances 0.000 claims description 2
- LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical compound [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 claims description 2
- FZGHWGNQHDJBME-UHFFFAOYSA-N C(C=1C(C(=O)OC)=CC=CC1)(=O)OC.[S] Chemical group C(C=1C(C(=O)OC)=CC=CC1)(=O)OC.[S] FZGHWGNQHDJBME-UHFFFAOYSA-N 0.000 claims 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 claims 1
- 239000000460 chlorine Substances 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- WFKAJVHLWXSISD-UHFFFAOYSA-N isobutyramide Chemical compound CC(C)C(N)=O WFKAJVHLWXSISD-UHFFFAOYSA-N 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 abstract description 5
- 239000002994 raw material Substances 0.000 abstract description 4
- 238000003512 Claisen condensation reaction Methods 0.000 abstract description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 235000019441 ethanol Nutrition 0.000 description 4
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 4
- 238000003786 synthesis reaction Methods 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 125000000687 hydroquinonyl group Chemical group C1(O)=C(C=C(O)C=C1)* 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
- 229910002666 PdCl2 Inorganic materials 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 2
- 238000001514 detection method Methods 0.000 description 2
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 238000004817 gas chromatography Methods 0.000 description 2
- 150000002561 ketenes Chemical class 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 235000011150 stannous chloride Nutrition 0.000 description 2
- TXUICONDJPYNPY-UHFFFAOYSA-N (1,10,13-trimethyl-3-oxo-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) heptanoate Chemical compound C1CC2CC(=O)C=C(C)C2(C)C2C1C1CCC(OC(=O)CCCCCC)C1(C)CC2 TXUICONDJPYNPY-UHFFFAOYSA-N 0.000 description 1
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N 1,4-Benzenediol Natural products OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 1
- FWWXYLGCHHIKNY-UHFFFAOYSA-N 2-ethoxyethyl prop-2-enoate Chemical compound CCOCCOC(=O)C=C FWWXYLGCHHIKNY-UHFFFAOYSA-N 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-N Formic acid Chemical class OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 1
- 229910021626 Tin(II) chloride Inorganic materials 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 150000004651 carbonic acid esters Chemical class 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 1
- UXGNZZKBCMGWAZ-UHFFFAOYSA-N dimethylformamide dmf Chemical compound CN(C)C=O.CN(C)C=O UXGNZZKBCMGWAZ-UHFFFAOYSA-N 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- PIBWKRNGBLPSSY-UHFFFAOYSA-L palladium(II) chloride Chemical compound Cl[Pd]Cl PIBWKRNGBLPSSY-UHFFFAOYSA-L 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 238000004321 preservation Methods 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- FKRCODPIKNYEAC-UHFFFAOYSA-N propionic acid ethyl ester Natural products CCOC(=O)CC FKRCODPIKNYEAC-UHFFFAOYSA-N 0.000 description 1
- UORVCLMRJXCDCP-UHFFFAOYSA-M propynoate Chemical compound [O-]C(=O)C#C UORVCLMRJXCDCP-UHFFFAOYSA-M 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000001119 stannous chloride Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/30—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
- C07C67/31—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by introduction of functional groups containing oxygen only in singly bound form
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/30—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
- C07C67/333—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton
- C07C67/343—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
Abstract
Description
Claims (7)
Priority Applications (1)
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CN201810119820.0A CN108299197B (zh) | 2018-02-06 | 2018-02-06 | 一种3-烷氧基丙烯酸酯合成方法 |
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CN201810119820.0A CN108299197B (zh) | 2018-02-06 | 2018-02-06 | 一种3-烷氧基丙烯酸酯合成方法 |
Publications (2)
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CN108299197A true CN108299197A (zh) | 2018-07-20 |
CN108299197B CN108299197B (zh) | 2021-08-03 |
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111153799A (zh) * | 2020-01-20 | 2020-05-15 | 浙江本立科技股份有限公司 | 3-甲氧基丙烯酸甲酯的制备方法 |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1088908A (zh) * | 1992-08-27 | 1994-07-06 | 曾尼卡有限公司 | 制备2-(2-甲基苯基)-3-甲氧基丙烯酸甲酯的化学方法 |
CN1206401A (zh) * | 1996-02-17 | 1999-01-27 | 巴斯福股份公司 | 2-(2-甲基苯基)-3-甲氧基丙烯酸甲酯的制备方法 |
WO2001018003A1 (en) * | 1999-09-10 | 2001-03-15 | Stichting Rega Vzw | Carbocyclic nucleosides and process for obtaining such |
CN101381305A (zh) * | 2008-10-21 | 2009-03-11 | 江苏耕耘化学有限公司 | 杀菌剂中间体(e)-2-(2'-溴甲基)苯基-3-甲氧基丙烯酸甲酯的制备方法 |
CN101781201A (zh) * | 2009-06-26 | 2010-07-21 | 上海海事大学 | 一种合成3-烷氧基丙烯酸酯的改进工艺 |
CN102746156A (zh) * | 2012-05-31 | 2012-10-24 | 上海海事大学 | 一种生产3-甲氧基丙烯酸甲酯的工艺 |
-
2018
- 2018-02-06 CN CN201810119820.0A patent/CN108299197B/zh active Active
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1088908A (zh) * | 1992-08-27 | 1994-07-06 | 曾尼卡有限公司 | 制备2-(2-甲基苯基)-3-甲氧基丙烯酸甲酯的化学方法 |
CN1206401A (zh) * | 1996-02-17 | 1999-01-27 | 巴斯福股份公司 | 2-(2-甲基苯基)-3-甲氧基丙烯酸甲酯的制备方法 |
WO2001018003A1 (en) * | 1999-09-10 | 2001-03-15 | Stichting Rega Vzw | Carbocyclic nucleosides and process for obtaining such |
CN101381305A (zh) * | 2008-10-21 | 2009-03-11 | 江苏耕耘化学有限公司 | 杀菌剂中间体(e)-2-(2'-溴甲基)苯基-3-甲氧基丙烯酸甲酯的制备方法 |
CN101781201A (zh) * | 2009-06-26 | 2010-07-21 | 上海海事大学 | 一种合成3-烷氧基丙烯酸酯的改进工艺 |
CN102746156A (zh) * | 2012-05-31 | 2012-10-24 | 上海海事大学 | 一种生产3-甲氧基丙烯酸甲酯的工艺 |
Non-Patent Citations (5)
Title |
---|
CARINE GUÉROT: "Construction of carbocycles via oxonium ylidesgeneration and rearrangement: towards the synthesis of taxol", 《UNIVERSITY OF GLASGOW PHD》 * |
CHAO ZHAO等: "Design and synthesis of novel androgen receptor antagonists via molecular modeling", 《BIOORGANIC & MEDICINAL CHEMISTRY》 * |
JAGADEESHWAR R. RAO等: "Enantioselective synthesis and antiviral activity of purine and pyrimidine cyclopentenyl C-nucleosides", 《BIOORGANIC & MEDICINAL CHEMISTRY》 * |
张开诚: "《大学化学实验 下》", 31 January 2011, 华中科技大学出版社 * |
董领娇: "伪异胞苷类化合物的合成", 《高等学校化学学报》 * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111153799A (zh) * | 2020-01-20 | 2020-05-15 | 浙江本立科技股份有限公司 | 3-甲氧基丙烯酸甲酯的制备方法 |
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