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4-[4-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)-phenyl]-[2,2']bipyridinyl

Base Information
  • Chemical Name:4-[4-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)-phenyl]-[2,2']bipyridinyl
  • CAS No.:858098-79-0
  • Molecular Formula:C22H23BN2O2
  • Molecular Weight:358.248
  • Hs Code.:
4-[4-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)-phenyl]-[2,2']bipyridinyl

Synonyms:4-[4-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)-phenyl]-[2,2']bipyridinyl

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Chemical Property of 4-[4-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)-phenyl]-[2,2']bipyridinyl
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Technology Process of 4-[4-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)-phenyl]-[2,2']bipyridinyl

There total 1 articles about 4-[4-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)-phenyl]-[2,2']bipyridinyl which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With potassium acetate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In dimethyl sulfoxide; under N2 atm. to soln. bpy-Ph-Br, K2CO3, and bis(pinacolato)diboron in DMSO PdCl2(dppf) was added and heated to 105°C for 17 h; react. mixt. was cooled to room temp., water was added, extd. with CH2Cl2, org. phase was evapd. in vacuo, residue was extd. with hexane;
DOI:10.1021/ic0483141
Guidance literature:
With K2CO3; tetrakis(triphenylphosphine) palladium(0); In N,N-dimethyl-formamide; under N2 atm. Pd(PPh3)4 was added to mixt. Ru complex, bpy-ph-B(OR)2, K2CO3 and DMF, heated at 120°C for 24 h, solvent was evapd., residue was dissolved in water/acetone (10:1), aq. soln. NH4PF6 was added; acetone was removed in vacuo, ppt. was filtered, washed with water and Et2O, purified on silica column with MeCN/H2O/MeOH/KNO3, 4:1:1:0.1 as eluent + product was purified by preparative tlc (SiO2), recrystn. from acetone/hexane;
DOI:10.1021/ic0483141
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