CN106631701A - 负载酸催化剂催化1、4‑桉叶素合成4‑松油醇的方法 - Google Patents
负载酸催化剂催化1、4‑桉叶素合成4‑松油醇的方法 Download PDFInfo
- Publication number
- CN106631701A CN106631701A CN201710018797.1A CN201710018797A CN106631701A CN 106631701 A CN106631701 A CN 106631701A CN 201710018797 A CN201710018797 A CN 201710018797A CN 106631701 A CN106631701 A CN 106631701A
- Authority
- CN
- China
- Prior art keywords
- acid catalyst
- terpineol
- cineoles
- supported acid
- modenite
- 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
- WRYLYDPHFGVWKC-UHFFFAOYSA-N 4-terpineol Chemical compound CC(C)C1(O)CCC(C)=CC1 WRYLYDPHFGVWKC-UHFFFAOYSA-N 0.000 title claims abstract description 91
- WRYLYDPHFGVWKC-SNVBAGLBSA-N 4-Terpineol Natural products CC(C)[C@]1(O)CCC(C)=CC1 WRYLYDPHFGVWKC-SNVBAGLBSA-N 0.000 title claims abstract description 46
- 239000003377 acid catalyst Substances 0.000 title claims abstract description 39
- 238000000034 method Methods 0.000 title claims abstract description 22
- 230000002194 synthesizing effect Effects 0.000 title abstract description 4
- RFFOTVCVTJUTAD-AOOOYVTPSA-N 1,4-cineole Chemical compound CC(C)[C@]12CC[C@](C)(CC1)O2 RFFOTVCVTJUTAD-AOOOYVTPSA-N 0.000 title abstract 4
- RFFOTVCVTJUTAD-UHFFFAOYSA-N cineole Natural products C1CC2(C)CCC1(C(C)C)O2 RFFOTVCVTJUTAD-UHFFFAOYSA-N 0.000 title abstract 4
- 238000006243 chemical reaction Methods 0.000 claims abstract description 20
- 239000003054 catalyst Substances 0.000 claims abstract description 7
- 230000035484 reaction time Effects 0.000 claims abstract description 3
- 125000000191 1,4-cineol group Chemical group 0.000 claims description 19
- 239000002253 acid Substances 0.000 claims description 14
- 238000003756 stirring Methods 0.000 claims description 13
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 12
- 238000006555 catalytic reaction Methods 0.000 claims description 11
- 239000000243 solution Substances 0.000 claims description 8
- 239000001117 sulphuric acid Substances 0.000 claims description 8
- 235000011149 sulphuric acid Nutrition 0.000 claims description 8
- 238000001514 detection method Methods 0.000 claims description 6
- 238000001914 filtration Methods 0.000 claims description 6
- 239000007788 liquid Substances 0.000 claims description 6
- 238000005292 vacuum distillation Methods 0.000 claims description 6
- 239000012153 distilled water Substances 0.000 claims description 5
- 239000012467 final product Substances 0.000 claims description 5
- 239000011259 mixed solution Substances 0.000 claims description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 5
- 238000011010 flushing procedure Methods 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- YKFLAYDHMOASIY-UHFFFAOYSA-N γ-terpinene Chemical compound CC(C)C1=CCC(C)=CC1 YKFLAYDHMOASIY-UHFFFAOYSA-N 0.000 abstract description 12
- YHQGMYUVUMAZJR-UHFFFAOYSA-N α-terpinene Chemical compound CC(C)C1=CC=C(C)CC1 YHQGMYUVUMAZJR-UHFFFAOYSA-N 0.000 abstract description 4
- 230000008569 process Effects 0.000 abstract description 3
- WSTYNZDAOAEEKG-UHFFFAOYSA-N Mayol Natural products CC1=C(O)C(=O)C=C2C(CCC3(C4CC(C(CC4(CCC33C)C)=O)C)C)(C)C3=CC=C21 WSTYNZDAOAEEKG-UHFFFAOYSA-N 0.000 abstract description 2
- 230000008901 benefit Effects 0.000 abstract description 2
- 229910052680 mordenite Inorganic materials 0.000 abstract 1
- 239000003921 oil Substances 0.000 description 17
- XFNJVJPLKCPIBV-UHFFFAOYSA-N trimethylenediamine Chemical compound NCCCN XFNJVJPLKCPIBV-UHFFFAOYSA-N 0.000 description 6
- 239000000047 product Substances 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
- 150000001336 alkenes Chemical class 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 239000000575 pesticide Substances 0.000 description 4
- 239000000376 reactant Substances 0.000 description 4
- 238000003786 synthesis reaction Methods 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 3
- 230000000844 anti-bacterial effect Effects 0.000 description 3
- 229910052744 lithium Inorganic materials 0.000 description 3
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- MOYAFQVGZZPNRA-UHFFFAOYSA-N Terpinolene Chemical compound CC(C)=C1CCC(C)=CC1 MOYAFQVGZZPNRA-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 230000004071 biological effect Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 150000002118 epoxides Chemical class 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 230000004044 response Effects 0.000 description 2
- 238000010189 synthetic method Methods 0.000 description 2
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
- FAMJUFMHYAFYNU-UHFFFAOYSA-N 1-methyl-4-(propan-2-yl)cyclohex-1-ene Chemical compound CC(C)C1CCC(C)=CC1 FAMJUFMHYAFYNU-UHFFFAOYSA-N 0.000 description 1
- NHQDETIJWKXCTC-UHFFFAOYSA-N 3-chloroperbenzoic acid Chemical compound OOC(=O)C1=CC=CC(Cl)=C1 NHQDETIJWKXCTC-UHFFFAOYSA-N 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 241000366182 Melaleuca alternifolia Species 0.000 description 1
- 244000269722 Thea sinensis Species 0.000 description 1
- 235000006468 Thea sinensis Nutrition 0.000 description 1
- 241000030601 Thuja standishii Species 0.000 description 1
- 241000700605 Viruses Species 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 230000003115 biocidal effect Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000012847 fine chemical Substances 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 229910000103 lithium hydride Inorganic materials 0.000 description 1
- LULAYUGMBFYYEX-UHFFFAOYSA-N metachloroperbenzoic acid Natural products OC(=O)C1=CC=CC(Cl)=C1 LULAYUGMBFYYEX-UHFFFAOYSA-N 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229930003647 monocyclic monoterpene Natural products 0.000 description 1
- -1 monocyclic monoterpene enol Chemical class 0.000 description 1
- 238000006396 nitration reaction Methods 0.000 description 1
- 229940055577 oleyl alcohol Drugs 0.000 description 1
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 238000012805 post-processing Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 235000013599 spices Nutrition 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 239000010677 tea tree oil Substances 0.000 description 1
- 229940111630 tea tree oil Drugs 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 239000000606 toothpaste Substances 0.000 description 1
- 229940034610 toothpaste Drugs 0.000 description 1
- LALRXNPLTWZJIJ-UHFFFAOYSA-N triethylborane Chemical group CCB(CC)CC LALRXNPLTWZJIJ-UHFFFAOYSA-N 0.000 description 1
- 239000000341 volatile oil Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/09—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrolysis
- C07C29/10—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrolysis of ethers, including cyclic ethers, e.g. oxiranes
- C07C29/103—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrolysis of ethers, including cyclic ethers, e.g. oxiranes of cyclic ethers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J29/00—Catalysts comprising molecular sieves
- B01J29/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
- B01J29/06—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
- B01J29/18—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the mordenite type
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/584—Recycling of catalysts
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
Description
Claims (9)
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CN201710018797.1A CN106631701B (zh) | 2017-01-11 | 2017-01-11 | 负载酸催化剂催化1、4-桉叶素合成4-松油醇的方法 |
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CN201710018797.1A CN106631701B (zh) | 2017-01-11 | 2017-01-11 | 负载酸催化剂催化1、4-桉叶素合成4-松油醇的方法 |
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CN106631701A true CN106631701A (zh) | 2017-05-10 |
CN106631701B CN106631701B (zh) | 2020-04-03 |
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Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108947767A (zh) * | 2018-06-18 | 2018-12-07 | 苏州盖德精细材料有限公司 | 4-松油醇的高效制备方法 |
CN109157426A (zh) * | 2018-10-15 | 2019-01-08 | 王杰 | 一种含有4-松油醇的皮肤护理剂及其制备方法 |
CN110054548A (zh) * | 2019-04-11 | 2019-07-26 | 中国农业科学院兰州畜牧与兽药研究所 | 一种固体酸凹凸棒催化合成4-松油醇的方法 |
CN110651797A (zh) * | 2018-06-28 | 2020-01-07 | 云南森美达生物科技有限公司 | 一种植物提取物、复配植物源杀虫剂及制备方法、应用 |
CN112473644A (zh) * | 2020-12-18 | 2021-03-12 | 云南森美达生物科技股份有限公司 | 负载型催化剂、制备方法及其用于γ-松油烯的制备方法 |
CN113980030A (zh) * | 2021-08-09 | 2022-01-28 | 江西农业大学 | 一种高选择性催化合成1,8-桉叶素的方法 |
CN114230575A (zh) * | 2021-12-07 | 2022-03-25 | 南昌工程学院 | 无溶剂体系催化α-松油醇合成1,8-桉叶素的方法 |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0152757A2 (en) * | 1984-01-16 | 1985-08-28 | Union Camp Corporation | Preparation of terpinen-4-ol |
CN102641743A (zh) * | 2012-04-13 | 2012-08-22 | 浙江师范大学 | 一种用于正构烷烃临氢异构化反应的催化剂及其制备方法和应用 |
-
2017
- 2017-01-11 CN CN201710018797.1A patent/CN106631701B/zh active Active
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0152757A2 (en) * | 1984-01-16 | 1985-08-28 | Union Camp Corporation | Preparation of terpinen-4-ol |
CN102641743A (zh) * | 2012-04-13 | 2012-08-22 | 浙江师范大学 | 一种用于正构烷烃临氢异构化反应的催化剂及其制备方法和应用 |
Non-Patent Citations (1)
Title |
---|
野村正人等: "シネオール類の合成ゼオライト存在下での酸による分解反応", 《日本化学会誌》 * |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108947767A (zh) * | 2018-06-18 | 2018-12-07 | 苏州盖德精细材料有限公司 | 4-松油醇的高效制备方法 |
CN108947767B (zh) * | 2018-06-18 | 2021-11-02 | 苏州盖德精细材料有限公司 | 4-松油醇的高效制备方法 |
CN110651797A (zh) * | 2018-06-28 | 2020-01-07 | 云南森美达生物科技有限公司 | 一种植物提取物、复配植物源杀虫剂及制备方法、应用 |
CN109157426A (zh) * | 2018-10-15 | 2019-01-08 | 王杰 | 一种含有4-松油醇的皮肤护理剂及其制备方法 |
CN110054548A (zh) * | 2019-04-11 | 2019-07-26 | 中国农业科学院兰州畜牧与兽药研究所 | 一种固体酸凹凸棒催化合成4-松油醇的方法 |
CN112473644A (zh) * | 2020-12-18 | 2021-03-12 | 云南森美达生物科技股份有限公司 | 负载型催化剂、制备方法及其用于γ-松油烯的制备方法 |
CN113980030A (zh) * | 2021-08-09 | 2022-01-28 | 江西农业大学 | 一种高选择性催化合成1,8-桉叶素的方法 |
CN114230575A (zh) * | 2021-12-07 | 2022-03-25 | 南昌工程学院 | 无溶剂体系催化α-松油醇合成1,8-桉叶素的方法 |
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Address after: 675100 Shuangbai County Industrial Park, Shuangbai County, Chuxiong Yi Autonomous Prefecture, Yunnan Province Patentee after: Yunnan senmeida Biotechnology Co.,Ltd. Address before: 675100 Shuangbai County, Chuxiong Yi Autonomous Prefecture, Yunnan County Industrial Park Patentee before: YUNNAN SENMEIDA BIOTECHNOLOGY Co.,Ltd. |
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Denomination of invention: Synthesis of 4-terpineol from 1,4-cineole catalyzed by supported acid catalyst Effective date of registration: 20221128 Granted publication date: 20200403 Pledgee: Kunming Dongfeng Sub branch of Bank of China Ltd. Pledgor: Yunnan senmeida Biotechnology Co.,Ltd. Registration number: Y2022530000036 |
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Denomination of invention: Method for catalytic synthesis of 4-terpineol from 1,4-eucalyptol using loaded acid catalysts Granted publication date: 20200403 Pledgee: Kunming Dongfeng Sub branch of Bank of China Ltd. Pledgor: Yunnan senmeida Biotechnology Co.,Ltd. Registration number: Y2024980010440 |
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