JP2018507871A5 - - Google Patents
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- Publication number
- JP2018507871A5 JP2018507871A5 JP2017546123A JP2017546123A JP2018507871A5 JP 2018507871 A5 JP2018507871 A5 JP 2018507871A5 JP 2017546123 A JP2017546123 A JP 2017546123A JP 2017546123 A JP2017546123 A JP 2017546123A JP 2018507871 A5 JP2018507871 A5 JP 2018507871A5
- Authority
- JP
- Japan
- Prior art keywords
- chloro
- compound
- formula
- ccl
- chcl
- 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
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- 239000000460 chlorine Substances 0.000 claims 45
- 229910052801 chlorine Inorganic materials 0.000 claims 40
- 150000001875 compounds Chemical class 0.000 claims 13
- 238000000034 method Methods 0.000 claims 10
- -1 3-chloro-2-methylphenoxy Chemical group 0.000 claims 9
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims 6
- 239000002585 base Substances 0.000 claims 5
- 239000002904 solvent Substances 0.000 claims 5
- SQIFRWXJZDVABQ-UHFFFAOYSA-N ClC=1C(=C(C=CC=1)O)C(C)O Chemical compound ClC=1C(=C(C=CC=1)O)C(C)O SQIFRWXJZDVABQ-UHFFFAOYSA-N 0.000 claims 4
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 claims 4
- MVTWVXYIKIVAOJ-UHFFFAOYSA-N 2-chloro-6-hydroxybenzaldehyde Chemical compound OC1=CC=CC(Cl)=C1C=O MVTWVXYIKIVAOJ-UHFFFAOYSA-N 0.000 claims 3
- HDYYBOSURIHFGM-UHFFFAOYSA-N 3-chloro-2-ethenylbenzenesulfonic acid Chemical class OS(=O)(=O)C1=CC=CC(Cl)=C1C=C HDYYBOSURIHFGM-UHFFFAOYSA-N 0.000 claims 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims 3
- 239000002253 acid Substances 0.000 claims 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 3
- 229910052700 potassium Inorganic materials 0.000 claims 3
- 229910052708 sodium Inorganic materials 0.000 claims 3
- ITQTTZVARXURQS-UHFFFAOYSA-N 3-methylpyridine Chemical compound CC1=CC=CN=C1 ITQTTZVARXURQS-UHFFFAOYSA-N 0.000 claims 2
- NTSLROIKFLNUIJ-UHFFFAOYSA-N 5-Ethyl-2-methylpyridine Chemical compound CCC1=CC=C(C)N=C1 NTSLROIKFLNUIJ-UHFFFAOYSA-N 0.000 claims 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 2
- 239000012320 chlorinating reagent Substances 0.000 claims 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 2
- ITIROJLQLPHMEQ-UHFFFAOYSA-N 3-chloro-2-ethenylphenol Chemical compound OC1=CC=CC(Cl)=C1C=C ITIROJLQLPHMEQ-UHFFFAOYSA-N 0.000 claims 1
- WADQOGCINABPRT-UHFFFAOYSA-N 3-chloro-2-methylphenol Chemical compound CC1=C(O)C=CC=C1Cl WADQOGCINABPRT-UHFFFAOYSA-N 0.000 claims 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
- BDAGIHXWWSANSR-UHFFFAOYSA-N Formic acid Chemical compound OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 claims 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims 1
- 230000002378 acidificating effect Effects 0.000 claims 1
- 239000003513 alkali Substances 0.000 claims 1
- 229910001854 alkali hydroxide Inorganic materials 0.000 claims 1
- 229910000288 alkali metal carbonate Inorganic materials 0.000 claims 1
- 150000008041 alkali metal carbonates Chemical class 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 claims 1
- 239000003153 chemical reaction reagent Substances 0.000 claims 1
- 235000019253 formic acid Nutrition 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 229910052744 lithium Inorganic materials 0.000 claims 1
- NXPHGHWWQRMDIA-UHFFFAOYSA-M magnesium;carbanide;bromide Chemical compound [CH3-].[Mg+2].[Br-] NXPHGHWWQRMDIA-UHFFFAOYSA-M 0.000 claims 1
- CCERQOYLJJULMD-UHFFFAOYSA-M magnesium;carbanide;chloride Chemical compound [CH3-].[Mg+2].[Cl-] CCERQOYLJJULMD-UHFFFAOYSA-M 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 claims 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000002524 organometallic group Chemical group 0.000 claims 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims 1
- WYURNTSHIVDZCO-UHFFFAOYSA-N tetrahydrofuran Substances C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims 1
- UCPYLLCMEDAXFR-UHFFFAOYSA-N triphosgene Chemical compound ClC(Cl)(Cl)OC(=O)OC(Cl)(Cl)Cl UCPYLLCMEDAXFR-UHFFFAOYSA-N 0.000 claims 1
- 239000008096 xylene Substances 0.000 claims 1
- 0 Cc(c(ClC)ccc1)c1O[N+](*)[O-] Chemical compound Cc(c(ClC)ccc1)c1O[N+](*)[O-] 0.000 description 2
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP15157832.5 | 2015-03-05 | ||
| EP15157832 | 2015-03-05 | ||
| PCT/EP2016/054189 WO2016139161A1 (en) | 2015-03-05 | 2016-02-29 | Process for preparing 3-chloro-2-vinylphenylsulfonates |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2018507871A JP2018507871A (ja) | 2018-03-22 |
| JP2018507871A5 true JP2018507871A5 (https=) | 2019-04-11 |
| JP6771475B2 JP6771475B2 (ja) | 2020-10-21 |
Family
ID=52736817
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017546123A Active JP6771475B2 (ja) | 2015-03-05 | 2016-02-29 | ３−クロロ−２−ビニルフェニルスルホネート類の製造方法 |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US10618872B2 (https=) |
| EP (1) | EP3265439B1 (https=) |
| JP (1) | JP6771475B2 (https=) |
| KR (1) | KR102595410B1 (https=) |
| CN (1) | CN107406374B (https=) |
| BR (1) | BR112017018993B1 (https=) |
| DK (1) | DK3265439T3 (https=) |
| ES (1) | ES2732045T3 (https=) |
| IL (1) | IL253877B (https=) |
| MX (1) | MX389099B (https=) |
| TW (1) | TWI695824B (https=) |
| WO (1) | WO2016139161A1 (https=) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3548463B1 (de) * | 2016-12-05 | 2020-10-14 | Bayer CropScience Aktiengesellschaft | Verfahren zur herstellung von 3-substituierten 2-vinylphenylsulfonaten |
| CN107043321B (zh) * | 2017-04-25 | 2021-01-15 | 连云港市工业投资集团有限公司 | 一种高选择性合成2,3-二氯苯甲醛的方法 |
| CN108911982B (zh) * | 2018-07-19 | 2022-08-26 | 徐州博康信息化学品有限公司 | 一种合成酰氧基取代的苯乙烯类化合物的环保方法 |
| CN111416150A (zh) * | 2020-02-28 | 2020-07-14 | 合肥国轩高科动力能源有限公司 | 一种含氟磺酸酯类锂离子电池添加剂的制备方法 |
| AR126600A1 (es) | 2021-07-29 | 2023-10-25 | Pi Industries Ltd | Compuestos novedosos de estireno y un proceso para la preparación de los mismos |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2109321T3 (es) | 1991-04-17 | 1998-01-16 | Rhone Poulenc Chimie | Intermedios de sintesis que presentan un ciclo hexanico y sus procedimientos de preparacion. |
| US5124460A (en) | 1991-05-06 | 1992-06-23 | Merck Sharp & Dohme Ltd. | Enantioselective synthesis of 3-substituted 1-azabicyclo (2.2.1)heptanes |
| JP2002515014A (ja) * | 1995-05-17 | 2002-05-21 | イー・アイ・デユポン・ドウ・ヌムール・アンド・カンパニー | 殺菌・殺カビ性の環式アミド類 |
| DE10021413A1 (de) | 2000-05-03 | 2001-11-08 | Bayer Ag | Verfahren zur Herstellung von 2-Alkyl-3-chlorphenolen |
| WO2010056631A1 (en) | 2008-11-12 | 2010-05-20 | Schering Corporation | Inhibitors of fatty acid binding protein (fabp) |
| EP2445891A4 (en) * | 2009-06-26 | 2012-11-14 | Glaxo Group Ltd | 5-CHAIN HETEROARYL DERIVATIVES AS SPHINOSINE-1-PHOSPHATE RECEPTOR AGONISTS |
| JP5785560B2 (ja) | 2009-12-21 | 2015-09-30 | バイエル・クロップサイエンス・アクチェンゲゼルシャフト | 殺真菌剤としてのビス（ジフルオロメチル）ピラゾール |
| JP2013522240A (ja) * | 2010-03-17 | 2013-06-13 | グラクソ グループ リミテッド | スフィンゴシン１−リン酸１（ｓ１ｐ１）受容体作用薬として用いるためのピリミジン誘導体 |
| WO2014207648A1 (en) * | 2013-06-24 | 2014-12-31 | Lupin Limited | Chromane and chromene derivatives and their use as crac modulators |
| JP6430494B2 (ja) | 2013-06-24 | 2018-11-28 | バイエル・クロップサイエンス・アクチェンゲゼルシャフト | 殺真菌剤としてのピペリジンカルボン酸誘導体 |
| TWI665192B (zh) * | 2014-05-28 | 2019-07-11 | 德商拜耳作物科學股份有限公司 | 製備二氫異唑衍生物之方法 |
-
2016
- 2016-02-29 KR KR1020177026671A patent/KR102595410B1/ko active Active
- 2016-02-29 DK DK16706865.9T patent/DK3265439T3/da active
- 2016-02-29 US US15/554,271 patent/US10618872B2/en active Active
- 2016-02-29 JP JP2017546123A patent/JP6771475B2/ja active Active
- 2016-02-29 CN CN201680013948.8A patent/CN107406374B/zh active Active
- 2016-02-29 BR BR112017018993-3A patent/BR112017018993B1/pt active IP Right Grant
- 2016-02-29 EP EP16706865.9A patent/EP3265439B1/en active Active
- 2016-02-29 ES ES16706865T patent/ES2732045T3/es active Active
- 2016-02-29 WO PCT/EP2016/054189 patent/WO2016139161A1/en not_active Ceased
- 2016-02-29 MX MX2017011389A patent/MX389099B/es unknown
- 2016-03-03 TW TW105106437A patent/TWI695824B/zh active
-
2017
- 2017-08-07 IL IL253877A patent/IL253877B/en active IP Right Grant
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