CN101851153B - 烯丙位氧化制备2-(6’-甲氧基-2’-萘基)烯丙醇的方法 - Google Patents
烯丙位氧化制备2-(6’-甲氧基-2’-萘基)烯丙醇的方法 Download PDFInfo
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- CN101851153B CN101851153B CN 201010198960 CN201010198960A CN101851153B CN 101851153 B CN101851153 B CN 101851153B CN 201010198960 CN201010198960 CN 201010198960 CN 201010198960 A CN201010198960 A CN 201010198960A CN 101851153 B CN101851153 B CN 101851153B
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- Prior art keywords
- naphthyl
- methoxyl group
- vinyl carbinol
- preparation
- propylene
- 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.)
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- 125000000746 allylic group Chemical group 0.000 title claims abstract description 12
- 238000000034 method Methods 0.000 title claims abstract description 12
- 238000007254 oxidation reaction Methods 0.000 title abstract description 12
- 230000003647 oxidation Effects 0.000 title abstract description 9
- DOKHEARVIDLSFF-UHFFFAOYSA-N prop-1-en-1-ol Chemical compound CC=CO DOKHEARVIDLSFF-UHFFFAOYSA-N 0.000 title abstract 3
- -1 benzyl carbamyl Chemical group 0.000 claims abstract description 31
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims abstract description 22
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims abstract description 20
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims abstract description 20
- 238000002360 preparation method Methods 0.000 claims abstract description 19
- 239000002608 ionic liquid Substances 0.000 claims abstract description 12
- 239000004342 Benzoyl peroxide Substances 0.000 claims abstract description 11
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 claims abstract description 11
- 235000019400 benzoyl peroxide Nutrition 0.000 claims abstract description 11
- 230000001590 oxidative effect Effects 0.000 claims abstract description 9
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims abstract description 5
- 229910001882 dioxygen Inorganic materials 0.000 claims abstract description 5
- 239000002994 raw material Substances 0.000 claims abstract description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 3
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 claims description 49
- 238000006243 chemical reaction Methods 0.000 claims description 34
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 21
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 12
- 239000003054 catalyst Substances 0.000 claims description 8
- 238000010898 silica gel chromatography Methods 0.000 claims description 8
- 238000003756 stirring Methods 0.000 claims description 8
- 238000000605 extraction Methods 0.000 claims description 7
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 6
- 239000007789 gas Substances 0.000 claims description 6
- 239000001301 oxygen Substances 0.000 claims description 6
- 229910052760 oxygen Inorganic materials 0.000 claims description 6
- 238000000926 separation method Methods 0.000 claims description 5
- 238000000746 purification Methods 0.000 claims description 4
- 238000001816 cooling Methods 0.000 claims description 2
- 238000003912 environmental pollution Methods 0.000 abstract description 2
- 230000003197 catalytic effect Effects 0.000 abstract 2
- 239000007800 oxidant agent Substances 0.000 abstract 2
- 238000005457 optimization Methods 0.000 abstract 1
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 21
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 7
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- CMWTZPSULFXXJA-UHFFFAOYSA-N Naproxen Natural products C1=C(C(C)C(O)=O)C=CC2=CC(OC)=CC=C21 CMWTZPSULFXXJA-UHFFFAOYSA-N 0.000 description 4
- 238000005516 engineering process Methods 0.000 description 4
- 229960002009 naproxen Drugs 0.000 description 4
- CMWTZPSULFXXJA-VIFPVBQESA-M naproxen(1-) Chemical compound C1=C([C@H](C)C([O-])=O)C=CC2=CC(OC)=CC=C21 CMWTZPSULFXXJA-VIFPVBQESA-M 0.000 description 4
- ACIAHEMYLLBZOI-ZZXKWVIFSA-N Unsaturated alcohol Chemical compound CC\C(CO)=C/C ACIAHEMYLLBZOI-ZZXKWVIFSA-N 0.000 description 3
- 150000001299 aldehydes Chemical class 0.000 description 3
- 150000002576 ketones Chemical class 0.000 description 3
- UFWIBTONFRDIAS-UHFFFAOYSA-N naphthalene-acid Natural products C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 3
- 238000010010 raising Methods 0.000 description 3
- 238000007341 Heck reaction Methods 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- 230000001760 anti-analgesic effect Effects 0.000 description 2
- 238000006356 dehydrogenation reaction Methods 0.000 description 2
- 235000019441 ethanol Nutrition 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 238000001953 recrystallisation Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 1
- 238000005160 1H NMR spectroscopy Methods 0.000 description 1
- KZDCMKVLEYCGQX-UDPGNSCCSA-N 2-(diethylamino)ethyl 4-aminobenzoate;(2s,5r,6r)-3,3-dimethyl-7-oxo-6-[(2-phenylacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid;hydrate Chemical class O.CCN(CC)CCOC(=O)C1=CC=C(N)C=C1.N([C@H]1[C@H]2SC([C@@H](N2C1=O)C(O)=O)(C)C)C(=O)CC1=CC=CC=C1 KZDCMKVLEYCGQX-UDPGNSCCSA-N 0.000 description 1
- VDWXOLWUMXBPHB-UHFFFAOYSA-N COc(cc1)cc(cc2)c1cc2C(CO)=C Chemical compound COc(cc1)cc(cc2)c1cc2C(CO)=C VDWXOLWUMXBPHB-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- 0 O=C(CC*1C=*(CCC(*c2ccccc2)=O)C=C1)*c1ccccc1 Chemical compound O=C(CC*1C=*(CCC(*c2ccccc2)=O)C=C1)*c1ccccc1 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 230000003110 anti-inflammatory effect Effects 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000007810 chemical reaction solvent Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 230000026030 halogenation Effects 0.000 description 1
- 238000005658 halogenation reaction Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 150000002460 imidazoles Chemical class 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- XYFCBTPGUUZFHI-UHFFFAOYSA-N phosphine group Chemical group P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 1
- QLNJFJADRCOGBJ-UHFFFAOYSA-N propionamide Chemical compound CCC(N)=O QLNJFJADRCOGBJ-UHFFFAOYSA-N 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 230000003637 steroidlike Effects 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
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- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Catalysts (AREA)
Abstract
Description
Claims (7)
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CN 201010198960 CN101851153B (zh) | 2010-06-12 | 2010-06-12 | 烯丙位氧化制备2-(6’-甲氧基-2’-萘基)烯丙醇的方法 |
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CN 201010198960 CN101851153B (zh) | 2010-06-12 | 2010-06-12 | 烯丙位氧化制备2-(6’-甲氧基-2’-萘基)烯丙醇的方法 |
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CN101851153A CN101851153A (zh) | 2010-10-06 |
CN101851153B true CN101851153B (zh) | 2013-01-16 |
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CN114292162B (zh) * | 2021-12-17 | 2023-11-03 | 江苏广域化学有限公司 | 3-氯-β-亚甲基苯乙醇类化合物及其中间体各自的制备方法 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5286902A (en) * | 1991-04-15 | 1994-02-15 | Koch Industries, Inc. | Process for preparation of 2-(6-methoxy-2-naphthyl)propionic acid and intermediates therefor utilizing 2,6-diisopropylnaphthalene |
CN1603294A (zh) * | 2004-08-11 | 2005-04-06 | 浙江工业大学 | 2-(6'-甲氧基-2'-萘基)烯丙醇的制备方法 |
CN101161617A (zh) * | 2007-11-15 | 2008-04-16 | 浙江工业大学 | 一种2-(6′-甲氧基-2'-萘基)烯丙醇的制备方法 |
CN101177381A (zh) * | 2007-11-28 | 2008-05-14 | 浙江工业大学 | 一种2-芳基烯丙醇化合物的合成方法 |
CN101204670A (zh) * | 2007-12-14 | 2008-06-25 | 浙江工业大学 | 一种氨基吡啶树脂负载钯催化剂及其应用 |
-
2010
- 2010-06-12 CN CN 201010198960 patent/CN101851153B/zh active Active
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5286902A (en) * | 1991-04-15 | 1994-02-15 | Koch Industries, Inc. | Process for preparation of 2-(6-methoxy-2-naphthyl)propionic acid and intermediates therefor utilizing 2,6-diisopropylnaphthalene |
CN1603294A (zh) * | 2004-08-11 | 2005-04-06 | 浙江工业大学 | 2-(6'-甲氧基-2'-萘基)烯丙醇的制备方法 |
CN101161617A (zh) * | 2007-11-15 | 2008-04-16 | 浙江工业大学 | 一种2-(6′-甲氧基-2'-萘基)烯丙醇的制备方法 |
CN101177381A (zh) * | 2007-11-28 | 2008-05-14 | 浙江工业大学 | 一种2-芳基烯丙醇化合物的合成方法 |
CN101204670A (zh) * | 2007-12-14 | 2008-06-25 | 浙江工业大学 | 一种氨基吡啶树脂负载钯催化剂及其应用 |
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Effective date of registration: 20171211 Address after: 313000 Zhejiang Province, Huzhou city Wuxing District Road No. 1188 district headquarters free port B building 14 Building 1403 room Patentee after: Zhejiang creation Intellectual Property Service Co., Ltd. Address before: Hangzhou City, Zhejiang province 310014 City Zhaohui District Six Patentee before: Zhejiang University of Technology |
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Effective date of registration: 20190103 Address after: No. 99, Tongshan University Road, Xuzhou, Jiangsu Province, Jiangsu Patentee after: XUZHOU LIFANG ELECTROMECHANICAL EQUIPMENT MANUFACTURING CO., LTD. Address before: 313000 1403, room 14, B building, free port, 1188 headquarters, Wuxing District, Huzhou, Zhejiang. Patentee before: Zhejiang creation Intellectual Property Service Co., Ltd. |
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Address after: No. 99 University Road, Xuzhou High-tech Zone, Jiangsu Province, 221000 Patentee after: XUZHOU LIFANG ELECTROMECHANICAL EQUIPMENT MANUFACTURING CO., LTD. Address before: 221000 No. 99 University Road, copper mountain, Jiangsu, Xuzhou Patentee before: XUZHOU LIFANG ELECTROMECHANICAL EQUIPMENT MANUFACTURING CO., LTD. |
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Application publication date: 20101006 Assignee: XUZHOU YIHU MACHINERY MANUFACTURING Co.,Ltd. Assignor: XUZHOU LIFANG MECHANICAL AND ELECTRICAL EQUIPMENT MANUFACTURING Co.,Ltd. Contract record no.: X2020980008293 Denomination of invention: Preparation of 2 - (6 '- methoxy-2' - naphthyl) allyl alcohol by allylic oxidation Granted publication date: 20130116 License type: Common License Record date: 20201120 |