JPWO2020235336A5 - - Google Patents
Download PDFInfo
- Publication number
- JPWO2020235336A5 JPWO2020235336A5 JP2021520691A JP2021520691A JPWO2020235336A5 JP WO2020235336 A5 JPWO2020235336 A5 JP WO2020235336A5 JP 2021520691 A JP2021520691 A JP 2021520691A JP 2021520691 A JP2021520691 A JP 2021520691A JP WO2020235336 A5 JPWO2020235336 A5 JP WO2020235336A5
- Authority
- JP
- Japan
- Prior art keywords
- solvent
- metal
- carbonate
- coordinating solvent
- compound
- 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
- 239000002904 solvent Substances 0.000 claims 18
- 229910052751 metal Inorganic materials 0.000 claims 12
- 239000002184 metal Substances 0.000 claims 12
- 150000001875 compounds Chemical class 0.000 claims 10
- 238000006243 chemical reaction Methods 0.000 claims 6
- 238000004519 manufacturing process Methods 0.000 claims 6
- 150000002739 metals Chemical class 0.000 claims 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical group CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims 3
- -1 aliphatic nitriles Chemical class 0.000 claims 3
- 150000003839 salts Chemical class 0.000 claims 3
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 claims 2
- OZJPLYNZGCXSJM-UHFFFAOYSA-N 5-valerolactone Chemical compound O=C1CCCCO1 OZJPLYNZGCXSJM-UHFFFAOYSA-N 0.000 claims 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 2
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical group COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 claims 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical group C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims 2
- 229910052783 alkali metal Inorganic materials 0.000 claims 2
- 150000001340 alkali metals Chemical class 0.000 claims 2
- JBTWLSYIZRCDFO-UHFFFAOYSA-N ethyl methyl carbonate Chemical compound CCOC(=O)OC JBTWLSYIZRCDFO-UHFFFAOYSA-N 0.000 claims 2
- FKRCODPIKNYEAC-UHFFFAOYSA-N ethyl propionate Chemical compound CCOC(=O)CC FKRCODPIKNYEAC-UHFFFAOYSA-N 0.000 claims 2
- KTQDYGVEEFGIIL-UHFFFAOYSA-N n-fluorosulfonylsulfamoyl fluoride Chemical compound FS(=O)(=O)NS(F)(=O)=O KTQDYGVEEFGIIL-UHFFFAOYSA-N 0.000 claims 2
- 150000002825 nitriles Chemical class 0.000 claims 2
- 150000003457 sulfones Chemical class 0.000 claims 2
- ZZXUZKXVROWEIF-UHFFFAOYSA-N 1,2-butylene carbonate Chemical group CCC1COC(=O)O1 ZZXUZKXVROWEIF-UHFFFAOYSA-N 0.000 claims 1
- WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 claims 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 claims 1
- UHOPWFKONJYLCF-UHFFFAOYSA-N 2-(2-sulfanylethyl)isoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(CCS)C(=O)C2=C1 UHOPWFKONJYLCF-UHFFFAOYSA-N 0.000 claims 1
- JWUJQDFVADABEY-UHFFFAOYSA-N 2-methyltetrahydrofuran Chemical group CC1CCCO1 JWUJQDFVADABEY-UHFFFAOYSA-N 0.000 claims 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims 1
- OIFBSDVPJOWBCH-UHFFFAOYSA-N Diethyl carbonate Chemical group CCOC(=O)OCC OIFBSDVPJOWBCH-UHFFFAOYSA-N 0.000 claims 1
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical group O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 claims 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical group [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 claims 1
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 claims 1
- 239000003660 carbonate based solvent Substances 0.000 claims 1
- 150000005678 chain carbonates Chemical class 0.000 claims 1
- 150000005676 cyclic carbonates Chemical class 0.000 claims 1
- 150000004292 cyclic ethers Chemical class 0.000 claims 1
- 125000004122 cyclic group Chemical group 0.000 claims 1
- SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical group COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 claims 1
- IEJIGPNLZYLLBP-UHFFFAOYSA-N dimethyl carbonate Chemical group COC(=O)OC IEJIGPNLZYLLBP-UHFFFAOYSA-N 0.000 claims 1
- 239000003759 ester based solvent Substances 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 239000004210 ether based solvent Substances 0.000 claims 1
- 229910021482 group 13 metal Inorganic materials 0.000 claims 1
- 150000004820 halides Chemical class 0.000 claims 1
- 239000003446 ligand Substances 0.000 claims 1
- 229910052749 magnesium Inorganic materials 0.000 claims 1
- 239000011777 magnesium Substances 0.000 claims 1
- 230000000737 periodic effect Effects 0.000 claims 1
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical group CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 claims 1
- 238000006467 substitution reaction Methods 0.000 claims 1
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 claims 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Chemical group C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims 1
- YFNKIDBQEZZDLK-UHFFFAOYSA-N triglyme Chemical group COCCOCCOCCOC YFNKIDBQEZZDLK-UHFFFAOYSA-N 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2019097130 | 2019-05-23 | ||
| JP2019097130 | 2019-05-23 | ||
| PCT/JP2020/018424 WO2020235336A1 (ja) | 2019-05-23 | 2020-05-01 | ビス（フルオロスルホニル）イミド化合物及びその製造方法 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JPWO2020235336A1 JPWO2020235336A1 (https=) | 2020-11-26 |
| JPWO2020235336A5 true JPWO2020235336A5 (https=) | 2022-01-13 |
| JP7266092B2 JP7266092B2 (ja) | 2023-04-27 |
Family
ID=73458400
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2021520691A Active JP7266092B2 (ja) | 2019-05-23 | 2020-05-01 | ビス（フルオロスルホニル）イミド化合物及びその製造方法 |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US12319571B2 (https=) |
| EP (1) | EP3967656B1 (https=) |
| JP (1) | JP7266092B2 (https=) |
| WO (1) | WO2020235336A1 (https=) |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8377406B1 (en) * | 2012-08-29 | 2013-02-19 | Boulder Ionics Corporation | Synthesis of bis(fluorosulfonyl)imide |
| JP6647877B2 (ja) | 2015-06-18 | 2020-02-14 | 株式会社日本触媒 | 非水電解液およびそれを用いた非水電解液二次電池 |
| US10020538B2 (en) | 2015-11-13 | 2018-07-10 | Uchicago Argonne, Llc | Salts for multivalent ion batteries |
| KR20180083896A (ko) | 2015-11-13 | 2018-07-23 | 론자 리미티드 | 비스(플루오로설포닐)-이미드 및 그 염의 제조 방법 |
| CN106430129A (zh) | 2016-08-30 | 2017-02-22 | 九江天赐高新材料有限公司 | 一种二氟磺酰亚胺盐的制备方法 |
-
2020
- 2020-05-01 JP JP2021520691A patent/JP7266092B2/ja active Active
- 2020-05-01 WO PCT/JP2020/018424 patent/WO2020235336A1/ja not_active Ceased
- 2020-05-01 EP EP20810728.4A patent/EP3967656B1/en active Active
- 2020-05-01 US US17/613,460 patent/US12319571B2/en active Active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Byun et al. | Cyclic sulfites and cyclic sulfates in organic synthesis | |
| JP2020511508A5 (https=) | ||
| CN103052592A (zh) | 从POF3或PF5制造LiPO2F2 | |
| JP2013539448A (ja) | ＬｉＰＯ２Ｆ２の製造 | |
| JP5716500B2 (ja) | （２Ｒ）−２−フルオロ−２−Ｃ−メチル−Ｄ−リボノ−γ−ラクトン類前駆体の製造方法 | |
| JP6174040B2 (ja) | トラボプロストの調製方法 | |
| KR100975520B1 (ko) | 마이코페놀레이트 모페틸의 개선된 제조방법 | |
| JPWO2020235336A5 (https=) | ||
| JP2010523647A (ja) | 安定した無水結晶形ドセタキセル及びその製造方法 | |
| CN105218488A (zh) | 一种卡非佐米中间体的制备方法及其中间体化合物 | |
| RU2012107136A (ru) | Способ получения простых полиэфироспиртов из алкиленоксидов | |
| CN108484543B (zh) | 一种穿琥宁或炎琥宁的制备方法 | |
| CN103450148A (zh) | 一种五元环硫酸酯化合物的合成方法 | |
| CN106366008B (zh) | 一种丙烯酸二酯类化合物及其制备方法 | |
| CN104478833A (zh) | 一种(s)-(+)-3-羟基四氢呋喃的合成方法 | |
| JP7707811B2 (ja) | アルキルフランカルボン酸エステルの製造方法 | |
| JP2011523631A5 (https=) | ||
| JP2011132072A (ja) | 六フッ化リン酸リチウムの製造方法 | |
| ES2682247T3 (es) | Síntesis quiral de N-{3,4-difluoro-2-[(2-fluoro-4-yodofenil)amino]-6-metoxifenil}-1-[2,3-dihidroxi-propil]ciclopropanosulfonamidas | |
| JPWO2023025776A5 (https=) | ||
| EP4493514A1 (en) | Process for manufacturing bis(fluorosulfonyl)imide salts | |
| RU2005106987A (ru) | Способ получения безводного хлорида марганца | |
| RU2007104036A (ru) | Способ получения диизопропил (гидроксиметил)-циклопропил)окси) метилфосфоната | |
| JP2014105182A (ja) | エーテル化合物製造法 | |
| KR102920871B1 (ko) | 플루오로에틸렌 카보네이트의 제조방법 |