CN108456155A - 用于制备含有氟磺酰基基团的酰亚胺盐的方法 - Google Patents
用于制备含有氟磺酰基基团的酰亚胺盐的方法 Download PDFInfo
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- CN108456155A CN108456155A CN201810199145.7A CN201810199145A CN108456155A CN 108456155 A CN108456155 A CN 108456155A CN 201810199145 A CN201810199145 A CN 201810199145A CN 108456155 A CN108456155 A CN 108456155A
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- 238000000034 method Methods 0.000 title claims abstract description 40
- -1 imide salts Chemical class 0.000 title claims abstract description 16
- 150000001875 compounds Chemical class 0.000 claims abstract description 28
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 claims abstract description 20
- 229910052731 fluorine Inorganic materials 0.000 claims abstract description 10
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims abstract description 8
- 239000003960 organic solvent Substances 0.000 claims abstract description 8
- 238000003682 fluorination reaction Methods 0.000 claims abstract description 7
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims abstract description 5
- 238000002360 preparation method Methods 0.000 claims abstract description 5
- 125000001453 quaternary ammonium group Chemical group 0.000 claims abstract description 5
- 150000001342 alkaline earth metals Chemical class 0.000 claims abstract description 4
- 125000006575 electron-withdrawing group Chemical group 0.000 claims abstract description 4
- 239000002904 solvent Substances 0.000 claims description 20
- 239000011877 solvent mixture Substances 0.000 claims description 13
- 238000006243 chemical reaction Methods 0.000 claims description 9
- 150000003839 salts Chemical class 0.000 claims description 9
- 238000009835 boiling Methods 0.000 claims description 8
- 229910052783 alkali metal Inorganic materials 0.000 claims description 5
- 150000001412 amines Chemical class 0.000 claims description 3
- 238000005341 cation exchange Methods 0.000 claims description 3
- 150000002148 esters Chemical class 0.000 claims description 3
- 150000002170 ethers Chemical class 0.000 claims description 3
- 150000002825 nitriles Chemical class 0.000 claims description 3
- 150000003003 phosphines Chemical class 0.000 claims description 3
- 239000010953 base metal Substances 0.000 claims description 2
- 239000003513 alkali Substances 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 9
- 230000015572 biosynthetic process Effects 0.000 description 5
- 239000000460 chlorine Substances 0.000 description 4
- 239000012429 reaction media Substances 0.000 description 4
- 238000003786 synthesis reaction Methods 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 3
- 238000000354 decomposition reaction Methods 0.000 description 3
- 150000003949 imides Chemical class 0.000 description 3
- XGZVUEUWXADBQD-UHFFFAOYSA-L lithium carbonate Chemical compound [Li+].[Li+].[O-]C([O-])=O XGZVUEUWXADBQD-UHFFFAOYSA-L 0.000 description 3
- 229910052808 lithium carbonate Inorganic materials 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000005086 pumping Methods 0.000 description 3
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
- 229910010941 LiFSI Inorganic materials 0.000 description 2
- 229910013870 LiPF 6 Inorganic materials 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 150000001450 anions Chemical class 0.000 description 2
- 150000001768 cations Chemical class 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 125000001153 fluoro group Chemical group F* 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- PQXKHYXIUOZZFA-UHFFFAOYSA-M lithium fluoride Chemical compound [Li+].[F-] PQXKHYXIUOZZFA-UHFFFAOYSA-M 0.000 description 2
- VDVLPSWVDYJFRW-UHFFFAOYSA-N lithium;bis(fluorosulfonyl)azanide Chemical compound [Li+].FS(=O)(=O)[N-]S(F)(=O)=O VDVLPSWVDYJFRW-UHFFFAOYSA-N 0.000 description 2
- YWWDBCBWQNCYNR-UHFFFAOYSA-N trimethylphosphine Chemical compound CP(C)C YWWDBCBWQNCYNR-UHFFFAOYSA-N 0.000 description 2
- 238000006677 Appel reaction Methods 0.000 description 1
- 229910017050 AsF3 Inorganic materials 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- 241001517013 Calidris pugnax Species 0.000 description 1
- 229910005143 FSO2 Inorganic materials 0.000 description 1
- 229910005187 FSO3Li Inorganic materials 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 230000003321 amplification Effects 0.000 description 1
- VMPVEPPRYRXYNP-UHFFFAOYSA-I antimony(5+);pentachloride Chemical compound Cl[Sb](Cl)(Cl)(Cl)Cl VMPVEPPRYRXYNP-UHFFFAOYSA-I 0.000 description 1
- 239000000010 aprotic solvent Substances 0.000 description 1
- JCMGUODNZMETBM-UHFFFAOYSA-N arsenic trifluoride Chemical compound F[As](F)F JCMGUODNZMETBM-UHFFFAOYSA-N 0.000 description 1
- 238000006664 bond formation reaction Methods 0.000 description 1
- JHRWWRDRBPCWTF-OLQVQODUSA-N captafol Chemical compound C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)C(Cl)Cl)C(=O)[C@H]21 JHRWWRDRBPCWTF-OLQVQODUSA-N 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- OWMJFBIZWDNTLY-UHFFFAOYSA-N diethyl(propan-2-yl)phosphane Chemical compound CCP(CC)C(C)C OWMJFBIZWDNTLY-UHFFFAOYSA-N 0.000 description 1
- 238000004146 energy storage Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- UQSQSQZYBQSBJZ-UHFFFAOYSA-N fluorosulfonic acid Chemical compound OS(F)(=O)=O UQSQSQZYBQSBJZ-UHFFFAOYSA-N 0.000 description 1
- ZTOMUSMDRMJOTH-UHFFFAOYSA-N glutaronitrile Chemical compound N#CCCCC#N ZTOMUSMDRMJOTH-UHFFFAOYSA-N 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 239000002608 ionic liquid Substances 0.000 description 1
- LRDFRRGEGBBSRN-UHFFFAOYSA-N isobutyronitrile Chemical compound CC(C)C#N LRDFRRGEGBBSRN-UHFFFAOYSA-N 0.000 description 1
- 229910001416 lithium ion Inorganic materials 0.000 description 1
- ULWOJODHECIZAU-UHFFFAOYSA-N n,n-diethylpropan-2-amine Chemical compound CCN(CC)C(C)C ULWOJODHECIZAU-UHFFFAOYSA-N 0.000 description 1
- PVMUVDSEICYOMA-UHFFFAOYSA-N n-chlorosulfonylsulfamoyl chloride Chemical compound ClS(=O)(=O)NS(Cl)(=O)=O PVMUVDSEICYOMA-UHFFFAOYSA-N 0.000 description 1
- 238000003199 nucleic acid amplification method Methods 0.000 description 1
- 230000003071 parasitic effect Effects 0.000 description 1
- FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 238000013341 scale-up Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- RXJKFRMDXUJTEX-UHFFFAOYSA-N triethylphosphine Chemical compound CCP(CC)CC RXJKFRMDXUJTEX-UHFFFAOYSA-N 0.000 description 1
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B21/00—Nitrogen; Compounds thereof
- C01B21/082—Compounds containing nitrogen and non-metals and optionally metals
- C01B21/086—Compounds containing nitrogen and non-metals and optionally metals containing one or more sulfur atoms
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B21/00—Nitrogen; Compounds thereof
- C01B21/082—Compounds containing nitrogen and non-metals and optionally metals
- C01B21/087—Compounds containing nitrogen and non-metals and optionally metals containing one or more hydrogen atoms
- C01B21/093—Compounds containing nitrogen and non-metals and optionally metals containing one or more hydrogen atoms containing also one or more sulfur atoms
- C01B21/0935—Imidodisulfonic acid; Nitrilotrisulfonic acid; Salts thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C303/00—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
- C07C303/36—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids
- C07C303/40—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids by reactions not involving the formation of sulfonamide groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR1261127A FR2998297B1 (fr) | 2012-11-22 | 2012-11-22 | Procede de preparation de sel d'imides contenant un groupement fluorosulfonyle |
| FR1261127 | 2012-11-22 | ||
| CN201380056760.8A CN104755418B (zh) | 2012-11-22 | 2013-11-19 | 用于制备含有氟磺酰基基团的酰亚胺盐的方法 |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201380056760.8A Division CN104755418B (zh) | 2012-11-22 | 2013-11-19 | 用于制备含有氟磺酰基基团的酰亚胺盐的方法 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN108456155A true CN108456155A (zh) | 2018-08-28 |
Family
ID=47557342
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201380056760.8A Active CN104755418B (zh) | 2012-11-22 | 2013-11-19 | 用于制备含有氟磺酰基基团的酰亚胺盐的方法 |
| CN201810199145.7A Pending CN108456155A (zh) | 2012-11-22 | 2013-11-19 | 用于制备含有氟磺酰基基团的酰亚胺盐的方法 |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201380056760.8A Active CN104755418B (zh) | 2012-11-22 | 2013-11-19 | 用于制备含有氟磺酰基基团的酰亚胺盐的方法 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US9725318B2 (enExample) |
| EP (2) | EP2922785B1 (enExample) |
| JP (2) | JP6339091B2 (enExample) |
| KR (1) | KR102118025B1 (enExample) |
| CN (2) | CN104755418B (enExample) |
| FR (1) | FR2998297B1 (enExample) |
| HU (1) | HUE038694T2 (enExample) |
| PL (1) | PL2922785T3 (enExample) |
| WO (1) | WO2014080120A1 (enExample) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP6691740B2 (ja) * | 2015-04-24 | 2020-05-13 | ステラケミファ株式会社 | フルオロスルホニルイミド化合物の製造方法 |
| JP2018514577A (ja) | 2015-05-06 | 2018-06-07 | ロンザ・リミテッド | ビス（フルオロスルホニル）−イミドの製造方法 |
| EP3090984A1 (en) | 2015-05-07 | 2016-11-09 | Lonza Ltd | Method for preparation of the salts of certain amines and bis(fluorosulfonyl)-imide |
| CN104925765B (zh) * | 2015-05-21 | 2017-08-08 | 上海康鹏科技有限公司 | 一种双氟磺酰亚胺锂盐的制备方法 |
| KR20180083896A (ko) * | 2015-11-13 | 2018-07-23 | 론자 리미티드 | 비스(플루오로설포닐)-이미드 및 그 염의 제조 방법 |
| US20190152792A1 (en) * | 2016-05-26 | 2019-05-23 | Morita Chemical Industries Co., Ltd. | Method for producing bis(fluorosulfonyl)imide alkali metal salt and bis(fluorosulfonyl)imide alkali metal salt composition |
| JP6663986B2 (ja) | 2016-05-27 | 2020-03-13 | 株式会社日本触媒 | ビス（フルオロスルホニル）イミドアルカリ金属塩の製造方法 |
| CN106219503B (zh) * | 2016-07-12 | 2018-11-30 | 武汉松石科技股份有限公司 | 一种双（氟磺酰）亚胺及其碱金属盐的制备方法 |
| JP2018035059A (ja) * | 2016-08-30 | 2018-03-08 | 森田化学工業株式会社 | リチウムビス（フルオロスルホニル）イミド組成物 |
| JP2018035060A (ja) * | 2016-08-30 | 2018-03-08 | 森田化学工業株式会社 | リチウムビス（フルオロスルホニル）イミド組成物 |
| FR3081456B1 (fr) * | 2018-05-23 | 2020-12-18 | Arkema France | Procede de preparation de sel d'imides contenant un groupement fluorosulfonyle |
| FR3081457B1 (fr) | 2018-05-23 | 2020-05-08 | Arkema France | Procede de preparation du sel de lithium du bis(fluorosulfonyl)imide |
| FR3081866B1 (fr) * | 2018-06-01 | 2020-05-08 | Arkema France | Procede de preparation de sel d'imides contenant un groupement fluorosulfonyle |
| CN109721037B (zh) | 2019-03-11 | 2019-12-24 | 上海如鲲新材料有限公司 | 一种双氟磺酰亚胺盐的新工艺 |
| US11267707B2 (en) | 2019-04-16 | 2022-03-08 | Honeywell International Inc | Purification of bis(fluorosulfonyl) imide |
| JP7346252B2 (ja) * | 2019-11-08 | 2023-09-19 | 株式会社日本触媒 | 非水電解液の製造方法及びリチウムイオン二次電池 |
| CN113104823A (zh) * | 2021-03-26 | 2021-07-13 | 广州理文科技有限公司 | 一种双（氟磺酰）亚胺的合成方法 |
| KR102677719B1 (ko) | 2021-07-08 | 2024-06-26 | 주식회사 천보 | 비스(플루오로술포닐)이미드 알칼리 금속염의 제조방법 |
| KR20250034311A (ko) | 2022-07-01 | 2025-03-11 | 스페셜티 오퍼레이션스 프랑스 | 기체 상의 수소 비스(클로로설포닐)이미드를 플루오르화하는 방법 |
| WO2025132313A1 (en) | 2023-12-20 | 2025-06-26 | Specialty Operations France | Method for fluorinating hydrogen bis(chlorosulfonyl)imide in gas phase |
| WO2025132314A1 (en) | 2023-12-20 | 2025-06-26 | Specialty Operations France | Method for fluorinating hydrogen bis(chlorosulfonyl)imide in gas phase |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20040097757A1 (en) * | 2000-12-29 | 2004-05-20 | Milos Cernik | Method for fluorinating a compound comprising a halosulphonyl or dihalophosphonyl group |
| CN101654229A (zh) * | 2009-09-04 | 2010-02-24 | 华中科技大学 | 一种制备含氟磺酰(磷酰)亚胺及其碱金属盐的方法 |
| CN102046523A (zh) * | 2008-07-23 | 2011-05-04 | 第一工业制药株式会社 | 双(氟磺酰基)亚胺阴离子化合物的制备方法和离子对化合物 |
| WO2011149095A1 (ja) * | 2010-05-28 | 2011-12-01 | 株式会社日本触媒 | フルオロスルホニルイミドのアルカリ金属塩およびその製造方法 |
| CN102617414A (zh) * | 2012-03-02 | 2012-08-01 | 苏州氟特电池材料有限公司 | 含氯磺酰/磷酰亚胺碱金属盐和含氟磺酰/磷酰亚胺碱金属盐的制备方法 |
| WO2012108284A1 (ja) * | 2011-02-10 | 2012-08-16 | 日本曹達株式会社 | フルオロスルホニルイミドアンモニウム塩の製造方法 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2183621C1 (ru) * | 2001-02-27 | 2002-06-20 | ГУП "Ангарский электролизный химический комбинат" | Способ получения фторангидридов сульфоновых кислот |
| US7919629B2 (en) | 2005-12-12 | 2011-04-05 | Phostech Lithium Inc. | Sulphonyl-1,2,4-triazole salts |
| WO2009123328A1 (en) | 2008-03-31 | 2009-10-08 | Nippon Shokubai Co., Ltd. | Sulfonylimide salt and method for producing the same |
| CN101503382A (zh) * | 2009-03-13 | 2009-08-12 | 中国科学院上海有机化学研究所 | 一种氟烷基磺酰亚胺及其氟烷基磺酰亚胺盐、制备方法和用途 |
| WO2012108384A1 (ja) * | 2011-02-10 | 2012-08-16 | シャープ株式会社 | 蛍光体基板、およびこれを用いた表示装置、照明装置 |
-
2012
- 2012-11-22 FR FR1261127A patent/FR2998297B1/fr not_active Expired - Fee Related
-
2013
- 2013-11-19 CN CN201380056760.8A patent/CN104755418B/zh active Active
- 2013-11-19 JP JP2015543497A patent/JP6339091B2/ja active Active
- 2013-11-19 CN CN201810199145.7A patent/CN108456155A/zh active Pending
- 2013-11-19 US US14/370,696 patent/US9725318B2/en active Active
- 2013-11-19 KR KR1020157016136A patent/KR102118025B1/ko active Active
- 2013-11-19 EP EP13815036.2A patent/EP2922785B1/fr active Active
- 2013-11-19 PL PL13815036T patent/PL2922785T3/pl unknown
- 2013-11-19 HU HUE13815036A patent/HUE038694T2/hu unknown
- 2013-11-19 WO PCT/FR2013/052785 patent/WO2014080120A1/fr not_active Ceased
- 2013-11-19 EP EP18172111.9A patent/EP3381889A1/fr not_active Withdrawn
-
2018
- 2018-05-08 JP JP2018089741A patent/JP2018172274A/ja active Pending
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20040097757A1 (en) * | 2000-12-29 | 2004-05-20 | Milos Cernik | Method for fluorinating a compound comprising a halosulphonyl or dihalophosphonyl group |
| CN102046523A (zh) * | 2008-07-23 | 2011-05-04 | 第一工业制药株式会社 | 双(氟磺酰基)亚胺阴离子化合物的制备方法和离子对化合物 |
| CN101654229A (zh) * | 2009-09-04 | 2010-02-24 | 华中科技大学 | 一种制备含氟磺酰(磷酰)亚胺及其碱金属盐的方法 |
| WO2011149095A1 (ja) * | 2010-05-28 | 2011-12-01 | 株式会社日本触媒 | フルオロスルホニルイミドのアルカリ金属塩およびその製造方法 |
| WO2012108284A1 (ja) * | 2011-02-10 | 2012-08-16 | 日本曹達株式会社 | フルオロスルホニルイミドアンモニウム塩の製造方法 |
| CN102617414A (zh) * | 2012-03-02 | 2012-08-01 | 苏州氟特电池材料有限公司 | 含氯磺酰/磷酰亚胺碱金属盐和含氟磺酰/磷酰亚胺碱金属盐的制备方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| FR2998297A1 (fr) | 2014-05-23 |
| HUE038694T2 (hu) | 2018-11-28 |
| JP6339091B2 (ja) | 2018-06-06 |
| PL2922785T3 (pl) | 2018-09-28 |
| JP2018172274A (ja) | 2018-11-08 |
| EP2922785A1 (fr) | 2015-09-30 |
| CN104755418A (zh) | 2015-07-01 |
| EP2922785B1 (fr) | 2018-06-27 |
| EP3381889A1 (fr) | 2018-10-03 |
| WO2014080120A1 (fr) | 2014-05-30 |
| KR20150085842A (ko) | 2015-07-24 |
| CN104755418B (zh) | 2018-04-13 |
| US9725318B2 (en) | 2017-08-08 |
| FR2998297B1 (fr) | 2014-11-14 |
| KR102118025B1 (ko) | 2020-06-02 |
| US20150246812A1 (en) | 2015-09-03 |
| JP2015536898A (ja) | 2015-12-24 |
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