JP2018518467A5 - - Google Patents
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- JP2018518467A5 JP2018518467A5 JP2017557332A JP2017557332A JP2018518467A5 JP 2018518467 A5 JP2018518467 A5 JP 2018518467A5 JP 2017557332 A JP2017557332 A JP 2017557332A JP 2017557332 A JP2017557332 A JP 2017557332A JP 2018518467 A5 JP2018518467 A5 JP 2018518467A5
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- 150000001875 compounds Chemical class 0.000 claims 26
- 238000000034 method Methods 0.000 claims 13
- 239000000203 mixture Substances 0.000 claims 11
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims 10
- 230000003647 oxidation Effects 0.000 claims 9
- 238000007254 oxidation reaction Methods 0.000 claims 9
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims 8
- 239000002808 molecular sieve Substances 0.000 claims 6
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 claims 6
- RZKSECIXORKHQS-UHFFFAOYSA-N Heptan-3-ol Chemical compound CCCCC(O)CC RZKSECIXORKHQS-UHFFFAOYSA-N 0.000 claims 4
- 239000002904 solvent Substances 0.000 claims 4
- MSXVEPNJUHWQHW-UHFFFAOYSA-N 2-methylbutan-2-ol Chemical compound CCC(C)(C)O MSXVEPNJUHWQHW-UHFFFAOYSA-N 0.000 claims 3
- 239000003054 catalyst Substances 0.000 claims 3
- 239000011541 reaction mixture Substances 0.000 claims 3
- NMRPBPVERJPACX-UHFFFAOYSA-N (3S)-octan-3-ol Natural products CCCCCC(O)CC NMRPBPVERJPACX-UHFFFAOYSA-N 0.000 claims 2
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 claims 2
- WOFPPJOZXUTRAU-UHFFFAOYSA-N 2-Ethyl-1-hexanol Natural products CCCCC(O)CCC WOFPPJOZXUTRAU-UHFFFAOYSA-N 0.000 claims 2
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 claims 2
- PFNHSEQQEPMLNI-UHFFFAOYSA-N 2-methyl-1-pentanol Chemical compound CCCC(C)CO PFNHSEQQEPMLNI-UHFFFAOYSA-N 0.000 claims 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 2
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 claims 2
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 claims 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 claims 2
- 239000008346 aqueous phase Substances 0.000 claims 2
- 239000007864 aqueous solution Substances 0.000 claims 2
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 claims 2
- PHTQWCKDNZKARW-UHFFFAOYSA-N isoamylol Chemical compound CC(C)CCO PHTQWCKDNZKARW-UHFFFAOYSA-N 0.000 claims 2
- 239000000463 material Substances 0.000 claims 2
- SJWFXCIHNDVPSH-UHFFFAOYSA-N octan-2-ol Chemical compound CCCCCCC(C)O SJWFXCIHNDVPSH-UHFFFAOYSA-N 0.000 claims 2
- 239000012074 organic phase Substances 0.000 claims 2
- 239000003960 organic solvent Substances 0.000 claims 2
- BVLCBFFLJLEBAA-UHFFFAOYSA-N 2,4,4-trimethylhexan-1-ol Chemical compound CCC(C)(C)CC(C)CO BVLCBFFLJLEBAA-UHFFFAOYSA-N 0.000 claims 1
- QEVWDMOIPOLQBL-UHFFFAOYSA-N 5-methyl-2-propylhexan-1-ol Chemical compound CCCC(CO)CCC(C)C QEVWDMOIPOLQBL-UHFFFAOYSA-N 0.000 claims 1
- HXQPUEQDBSPXTE-UHFFFAOYSA-N Diisobutylcarbinol Chemical compound CC(C)CC(O)CC(C)C HXQPUEQDBSPXTE-UHFFFAOYSA-N 0.000 claims 1
- 150000001298 alcohols Chemical class 0.000 claims 1
- 150000001335 aliphatic alkanes Chemical class 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 150000002170 ethers Chemical class 0.000 claims 1
- 230000007062 hydrolysis Effects 0.000 claims 1
- 238000006460 hydrolysis reaction Methods 0.000 claims 1
- 230000003301 hydrolyzing effect Effects 0.000 claims 1
- 150000002825 nitriles Chemical class 0.000 claims 1
- 239000012071 phase Substances 0.000 claims 1
- YLQLIQIAXYRMDL-UHFFFAOYSA-N propylheptyl alcohol Chemical compound CCCCCC(CO)CCC YLQLIQIAXYRMDL-UHFFFAOYSA-N 0.000 claims 1
- 230000035484 reaction time Effects 0.000 claims 1
- 238000000926 separation method Methods 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP15166260 | 2015-05-04 | ||
| EP15166260.8 | 2015-05-04 | ||
| PCT/EP2016/060062 WO2016177814A1 (en) | 2015-05-04 | 2016-05-04 | Process for the preparation of melonal |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2018518467A JP2018518467A (ja) | 2018-07-12 |
| JP2018518467A5 true JP2018518467A5 (https=) | 2019-06-06 |
| JP6741687B2 JP6741687B2 (ja) | 2020-08-19 |
Family
ID=53040424
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017557332A Active JP6741687B2 (ja) | 2015-05-04 | 2016-05-04 | メロナールの調製方法 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US10202324B2 (https=) |
| EP (1) | EP3292099B1 (https=) |
| JP (1) | JP6741687B2 (https=) |
| CN (1) | CN107735392B (https=) |
| ES (1) | ES2821890T3 (https=) |
| MX (1) | MX2017014148A (https=) |
| WO (1) | WO2016177814A1 (https=) |
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| JP6741687B2 (ja) | 2015-05-04 | 2020-08-19 | ビーエーエスエフ ソシエタス・ヨーロピアＢａｓｆ Ｓｅ | メロナールの調製方法 |
| BR112018000606B1 (pt) | 2015-07-22 | 2022-01-18 | Basf Se | Processo para preparação de ácido furan-2,5- dicarboxílico e uso de um catalisador |
| EP3170828A1 (de) * | 2015-11-23 | 2017-05-24 | Basf Se | Verfahren zur herstellung von verbindungen mit 16-oxabicyclo[10.3.1]pentadecengerüst und deren folgeprodukten |
| CN108290134A (zh) | 2015-11-27 | 2018-07-17 | 巴斯夫欧洲公司 | 金属-有机骨架的超快高空时产率合成 |
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| CN114292170B (zh) * | 2022-01-11 | 2023-01-13 | 万华化学集团股份有限公司 | 一种合成甜瓜醛的方法 |
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| US9950982B2 (en) | 2014-12-19 | 2018-04-24 | Basf Se (Reitstötter, Kinzebach & Partner) | 1-(7,10,10-trimethyl-4-bicyclo(6.2.0)decanyl)ethanone as novel aroma chemical |
| WO2016116406A1 (de) | 2015-01-21 | 2016-07-28 | Basf Se | Gasdruckbehälter enthaltend ein gas, ein latentwärmespeichermaterial und einen porösen feststoff |
| KR102558113B1 (ko) | 2015-02-12 | 2023-07-24 | 바스프 에스이 | Bea 골격 구조를 갖는 탈알루미늄화된 제올라이트 물질의 제조 방법 |
| JP6685315B2 (ja) | 2015-02-13 | 2020-04-22 | ビーエーエスエフ ソシエタス・ヨーロピアＢａｓｆ Ｓｅ | プロピレンのエポキシ化のためのチタンゼオライト触媒の再生方法 |
| WO2016135133A1 (en) | 2015-02-27 | 2016-09-01 | Basf Se | A vehicle comprising a storage system and a combustion engine, the storage system comprising a container and at least one storage vessel |
| CN107438600B (zh) | 2015-03-05 | 2021-04-13 | 巴斯夫欧洲公司 | 制备四氢吡喃基酯的方法 |
| DE102015103608A1 (de) | 2015-03-11 | 2016-09-15 | Basf Se | Verfahren zur mikrobiellen de novo Synthese von Terpenen |
| JP6741687B2 (ja) | 2015-05-04 | 2020-08-19 | ビーエーエスエフ ソシエタス・ヨーロピアＢａｓｆ Ｓｅ | メロナールの調製方法 |
-
2016
- 2016-05-04 JP JP2017557332A patent/JP6741687B2/ja active Active
- 2016-05-04 ES ES16722841T patent/ES2821890T3/es active Active
- 2016-05-04 MX MX2017014148A patent/MX2017014148A/es unknown
- 2016-05-04 EP EP16722841.0A patent/EP3292099B1/en active Active
- 2016-05-04 CN CN201680039475.9A patent/CN107735392B/zh active Active
- 2016-05-04 WO PCT/EP2016/060062 patent/WO2016177814A1/en not_active Ceased
- 2016-05-04 US US15/571,107 patent/US10202324B2/en active Active
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