Technology Process of 1,3-bis-(4-allyl-2,6-diisopropylphenyl)imidazolium chloride
There total 4 articles about 1,3-bis-(4-allyl-2,6-diisopropylphenyl)imidazolium chloride 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
water;
In
tetrahydrofuran;
at 40 ℃;
for 16h;
Schlenk technique;
Glovebox;
Inert atmosphere;
DOI:10.1039/c4gc00642a
- Guidance literature:
-
Multi-step reaction with 4 steps
1: 5,5-dimethyl-1,3-cyclohexadiene / 12 h / 120 °C / Schlenk technique; Glovebox; Inert atmosphere
2: zinc(II) chloride / 5,5-dimethyl-1,3-cyclohexadiene / 4 h / Reflux; Schlenk technique; Glovebox; Inert atmosphere
3: formic acid / isopropyl alcohol; water / Schlenk technique; Glovebox; Inert atmosphere
4: water / tetrahydrofuran / 16 h / 40 °C / Schlenk technique; Glovebox; Inert atmosphere
With
formic acid; water; zinc(II) chloride;
In
tetrahydrofuran; 5,5-dimethyl-1,3-cyclohexadiene; water; isopropyl alcohol;
2: |Aza-Claisen Rearrangement;
DOI:10.1039/c4gc00642a
- Guidance literature:
-
Multi-step reaction with 3 steps
1: zinc(II) chloride / 5,5-dimethyl-1,3-cyclohexadiene / 4 h / Reflux; Schlenk technique; Glovebox; Inert atmosphere
2: formic acid / isopropyl alcohol; water / Schlenk technique; Glovebox; Inert atmosphere
3: water / tetrahydrofuran / 16 h / 40 °C / Schlenk technique; Glovebox; Inert atmosphere
With
formic acid; water; zinc(II) chloride;
In
tetrahydrofuran; 5,5-dimethyl-1,3-cyclohexadiene; water; isopropyl alcohol;
1: |Aza-Claisen Rearrangement;
DOI:10.1039/c4gc00642a