Production Method 1

90076-65-6

959698-46-5

959698-43-2

98837-98-0

Reaction Conditions

1.1 Solvents: Ethanol ;  17 h, rt

Reference

Design of ionic liquids as a medium for the Grignard reaction

Itoh, Toshiyuki; Kude, Keisuke; Hayase, Shuichi; Kawatsura, Motoi, Tetrahedron Letters, 2007, 48(44), 7774-7777

Production Method 2

90076-65-6

959698-46-5

959698-43-2

98837-98-0

Reaction Conditions

1.1 Solvents: Ethanol ;  17 h, rt

Reference

Iron-catalyzed quick homocoupling reaction of aryl or alkynyl Grignard reagents using a phosphonium ionic liquid solvent system

Kude, Keisuke; Hayase, Shuichi; Kawatsura, Motoi; Itoh, Toshiyuki, Heteroatom Chemistry, 2011, 22(3-4), 397-404

Production Method 3

90076-65-6

959698-46-5

959698-43-2

98837-98-0

Reaction Conditions

1.1 Solvents: Ethanol ;  17 h, rt

Reference

Phosphonium-based ionic liquids and their uses as coupling reaction solvents for preparation of biaryl compounds

, Japan, , ,

Production Method 4

6482-24-2

998-40-3

82113-65-3

959698-43-2

98837-98-0

Reaction Conditions

1.1 Solvents: Ethanol ,  Hexane ;  22 h, 80 °C; 80 °C → rt
1.2 Solvents: Ethanol ;  17 h, rt

Reference

Design of phosphonium ionic liquids for lipase-catalyzed transesterification

Abe, Yoshikazu; Kude, Keisuke; Hayase, Shuichi; Kawatsura, Motoi; Tsunashima, Katsuhiko; et al, Journal of Molecular Catalysis B: Enzymatic, 2008, 51(3-4), 81-85

Production Method 5

90076-65-6

959698-46-5

959698-43-2

98837-98-0

Reaction Conditions

1.1 Solvents: Water ;  20 min, rt

Reference

Glycol-functionalized ionic liquids for high-temperature enzymatic ring-opening polymerization

Zhao, Hua; Afriyie, Lennox O.; Larm, Nathaniel E.; Baker, Gary A., RSC Advances, 2018, 8(63), 36025-36033

Production Method 6

6482-24-2

998-40-3

90076-65-6

959698-43-2

98837-98-0

Reaction Conditions

1.1 Solvents: Ethanol ;  22 h, 80 °C; 80 °C → rt
1.2 17 h, rt

Reference

Ionic conductors containing onium cations and polar substances, and electrochemical cells and fuel cells using them

, Japan, , ,

Phosphonium, tributyl(2-methoxyethyl)- Raw materials

• 1-Bromo-2-methoxyethane
• Tributyl Phosphine
• 1,1,1-Trifluoro-N-((trifluoromethyl)sulfonyl)methanesulfonamide
• Lithium bis(trifluoromethanesulphonyl)imide
• Phosphonium, tributyl(2-methoxyethyl)-, bromide (1:1)

Phosphonium, tributyl(2-methoxyethyl)- Preparation Products

• Phosphonium, tributyl(2-methoxyethyl)- (959698-43-2)
• N-Propyl-Methyl Piperidinium Bis(trifluoroMethylsulfonyl)Imide (98837-98-0)

• 1. Dissolved oxygen sensor based on fluorescence quenching of oxygen-sensitive ruthenium complexes immobilized in sol–gel-derived porous silica coatings
  Analyst, 1996,121, 785-788
• 2. Exchanged ligands on the surface of a giant cluster: [(MoO3)176(H2O)63(CH3OH)17Hn](32 – n)–
  Chem. Commun., 1998, 1501-1502
• 3. Fe(ii)-Assisted one-pot synthesis of ultra-small core–shell Au–Pt nanoparticles as superior catalysts towards the HER and ORR?
  Yi Cao,Yujiao Xiahou,Lixiang Xing,Xiang Zhang,Hong Li,ChenShou Wu,Haibing Xia Nanoscale, 2020,12, 20456-20466
• 4. Excited state dynamics of symmetric and asymmetric Cr3(dpa)4Cl2 measured using femtosecond transient absorption spectroscopy?
  Chao-Han Cheng,Wen-Zhen Wang,Shie-Ming Peng,I-Chia Chen Phys. Chem. Chem. Phys., 2017,19, 25471-25477
• 5. Fe/Fe3C@C nanoparticles encapsulated in N-doped graphene–CNTs framework as an efficient bifunctional oxygen electrocatalyst for robust rechargeable Zn–air batteries?
  Zhiyan Chen,Nan Wu,Yaobing Wang,Bing Wang,Yingde Wang J. Mater. Chem. A, 2018,6, 516-526

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