Synthesis of tetrabutylammonium bis(fluorosulfonyl)imide and related salts
원문보기
IPC분류정보
국가/구분
United States(US) Patent
등록
국제특허분류(IPC7판)
C07C-209/68
C07C-211/03
C07C-311/48
C01B-021/086
출원번호
US-0883054
(2015-10-14)
등록번호
US-9475764
(2016-10-25)
발명자
/ 주소
Johnson, Martin Reid
출원인 / 주소
Trinapco, Inc.
대리인 / 주소
Duane Morris LLP
인용정보
피인용 횟수 :
0인용 특허 :
12
초록▼
The present invention is directed to methods comprising adding ammonia, either as an ammonium salt or as a gas at pressures below 0.01 MPa, to a sulfuryl fluoride solution to form the anion of bis(fluorosulfonyl)amine under conditions well suited for large-scale production. The bis(fluorosulfonyl)am
The present invention is directed to methods comprising adding ammonia, either as an ammonium salt or as a gas at pressures below 0.01 MPa, to a sulfuryl fluoride solution to form the anion of bis(fluorosulfonyl)amine under conditions well suited for large-scale production. The bis(fluorosulfonyl)amine so produced can be isolated by methods described in the prior art, or isolated as an organic ion pair, such as an alkylammonium solid salt, or as an ionic liquid.
대표청구항▼
1. A process for producing a salt of bis(fluorosulfonyl) imide anion (Mx+m[(FSO2)2N−]n, wherein M+ is an inorganic or organic cation and x, n and m are integers from 1-4, comprising: adding sulfuryl fluoride (SO2F2) to solid ammonium fluoride in a solvent in a reactor, in the presence of an aprotic
1. A process for producing a salt of bis(fluorosulfonyl) imide anion (Mx+m[(FSO2)2N−]n, wherein M+ is an inorganic or organic cation and x, n and m are integers from 1-4, comprising: adding sulfuryl fluoride (SO2F2) to solid ammonium fluoride in a solvent in a reactor, in the presence of an aprotic base; andisolating said salt. 2. The process of claim 1, wherein the step of adding sulfuryl fluoride (SO2F2) to solid ammonium fluoride in a solvent in a reactor, in the presence of an aprotic base, comprises providing solid ammonium fluoride to the solvent in the reactor;providing the aprotic base and an initial amount of sulfuryl fluoride (SO2F2) in the reactor; andcontinuously adding an additional amount of SO2F2 to reach a pre-determined stoichiometry. 3. The process of claim 2, wherein the pre-determined stoichiometry of ammonium fluoride to SO2F2 is in a molar ratio in the range from 1:3 to 1.1:2. 4. The process of claim 1, wherein sulfuryl fluoride (SO2F2) is added to a suspension, pellet, or other form of solid ammonium fluoride in the solvent. 5. The process of claim 1, wherein the reactor is a sealed reactor. 6. The process of claim 5, further comprising applying vacuum to the sealed reactor. 7. The process of claim 1, wherein the solvent is selected from the group consisting of acetonitrile, propionitrile, diethyl ether, tetrahydrofuran, butyronitrile, dimethylformamide, dimethylacetamide, N-methylpyrrolidinone, tetramethylurea, dimethylpropyleneurea, dimethylethyleneurea and a combinations thereof. 8. The process of claim 1, wherein the aprotic base is N,N,N′,N′-tetramethyl-1,3-propanediamine. 9. The process of claim 1, wherein the reaction is maintained at a temperature in the range from −30° C. to +50° C. during the step of adding sulfuryl fluoride (SO2F2). 10. The process of claim 1, wherein the pressure within the reactor is at or below about 0.3 MPa during the step of adding sulfuryl fluoride (SO2F2). 11. The process of claim 1, wherein the pressure within the reactor is in the range from about 0.1 MPa to about 0.3 MPa during the step of adding sulfuryl fluoride (SO2F2). 12. The process of claim 1, wherein the pressure within the reactor is in the range from about 0.01 MPa to about 0.1 MPa during the step of adding sulfuryl fluoride (SO2F2). 13. The process of claim 1, further comprising a step of distilling the solvent. 14. The process of claim 1, wherein the step of isolating the resulting salt comprises adding a solution of a salt comprising an organic cation. 15. The process of claim 1, wherein the salt having the formula ([M]x+)m([(FSO2)2N]−)n is isolated as a solid, and is collected by filtration. 16. A process for producing a salt of bis(fluorosulfonyl) imide anion (Mx+m[(FSO2)2N−]n, wherein M+ is an inorganic or organic cation and x, n and m are integers from 1-4, comprising: mixing sulfuryl fluoride (SO2F2), solid ammonium fluoride, a solvent and an aprotic base in a sealed reactor; andisolating said salt. 17. The process of claim 16, wherein the step of mixing sulfuryl fluoride (SO2F2), solid ammonium fluoride, a solvent and an aprotic base in a sealed reactor, comprises providing solid ammonium fluoride to the solvent in the sealed reactor;providing the aprotic base and an initial amount of sulfuryl fluoride (SO2F2) in the reactor; andcontinuously adding an additional amount of SO2F2 to reach a pre-determined stoichiometry. 18. The process of claim 16, wherein the aprotic base is N,N,N′,N′-tetramethyl-1,3-propanediamine. 19. The process of claim 16, further comprising a step of distilling the solvent. 20. The process of claim 16, wherein the step of isolating the resulting salt comprises adding a solution of a salt comprising an organic cation.
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이 특허에 인용된 특허 (12)
Michot, Christophe; Armand, Michel; Sanchez, Jean-Yves; Choquette, Yves; Gauthier, Michel, Ionic conducting material having good anticorrosive properties.
Howells Richard D. ; Lamanna William M. ; Fanta Alan D. ; Waddell Jennifer, Preparation of bis (fluoroalkylenesulfonyl) imides and (fluoroalkysulfony) (fluorosulfonyl) imides.
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