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1,3-dimethylimidazolin-2-ylidene-tetrafluoro[4-(4-propylcyclohexyl)phenyl]phosphorane adduct

Base Information Edit
  • Chemical Name:1,3-dimethylimidazolin-2-ylidene-tetrafluoro[4-(4-propylcyclohexyl)phenyl]phosphorane adduct
  • CAS No.:1455481-88-5
  • Molecular Formula:C20H31F4N2P
  • Molecular Weight:406.447
  • Hs Code.:
  • Mol file:1455481-88-5.mol
1,3-dimethylimidazolin-2-ylidene-tetrafluoro[4-(4-propylcyclohexyl)phenyl]phosphorane adduct

Synonyms:1,3-dimethylimidazolin-2-ylidene-tetrafluoro[4-(4-propylcyclohexyl)phenyl]phosphorane adduct

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Chemical Property of 1,3-dimethylimidazolin-2-ylidene-tetrafluoro[4-(4-propylcyclohexyl)phenyl]phosphorane adduct Edit
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Technology Process of 1,3-dimethylimidazolin-2-ylidene-tetrafluoro[4-(4-propylcyclohexyl)phenyl]phosphorane adduct

There total 4 articles about 1,3-dimethylimidazolin-2-ylidene-tetrafluoro[4-(4-propylcyclohexyl)phenyl]phosphorane adduct 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:
Multi-step reaction with 4 steps
1: magnesium / tetrahydrofuran / 1 h / Inert atmosphere; Reflux
2: tetrahydrofuran / 16 h / -20 - 20 °C / Inert atmosphere
3: hydrogenchloride / diethyl ether / 20 °C / Inert atmosphere
4: tetrahydrofuran / 18 h / -40 - 20 °C / Inert atmosphere
With hydrogenchloride; magnesium; In tetrahydrofuran; diethyl ether;
DOI:10.1016/j.tet.2013.07.062
Guidance literature:
Multi-step reaction with 3 steps
1: tetrahydrofuran / 16 h / -20 - 20 °C / Inert atmosphere
2: hydrogenchloride / diethyl ether / 20 °C / Inert atmosphere
3: tetrahydrofuran / 18 h / -40 - 20 °C / Inert atmosphere
With hydrogenchloride; In tetrahydrofuran; diethyl ether;
DOI:10.1016/j.tet.2013.07.062
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