Technology Process of 7-[4-(6-Chlorocarbonyl-hexyl)-2,3,5,6-tetramethyl-phenyl]-heptanoyl chloride
There total 15 articles about 7-[4-(6-Chlorocarbonyl-hexyl)-2,3,5,6-tetramethyl-phenyl]-heptanoyl 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:
-
Multi-step reaction with 13 steps
1: 89.4 percent / cc. H2SO4 / toluene
2: 89.6 percent / B2H6 / tetrahydrofuran
3: 91.2 percent / 48 percent HBr / H2O / 0.5 h / Heating
4: 1.) Na / 1.) ethanol; 2.) ethanol, reflux
5: H2O, KOH / Heating
6: 94.6 percent / quinoline / 0.33 h / Heating
7: 95 percent / cc. H2SO4 / toluene
8: 99 percent / B2H6 / tetrahydrofuran
9: 86 percent / 48 percent HBr / H2O / 0.5 h / Heating
10: 1.) Na / 1.) ethanol; 2.) ethanol, reflux
11: H2O, KOH / Heating
12: diethylformamide / Heating
13: SOCl2 / Heating
With
quinoline; potassium hydroxide; thionyl chloride; N-ethylpropionamide; sulfuric acid; water; hydrogen bromide; sodium; diborane;
In
tetrahydrofuran; water; toluene;
- Guidance literature:
-
Multi-step reaction with 15 steps
1: H2O, KOH / Heating
2: 94.7 percent / quinoline / 0.33 h / Heating
3: 89.4 percent / cc. H2SO4 / toluene
4: 89.6 percent / B2H6 / tetrahydrofuran
5: 91.2 percent / 48 percent HBr / H2O / 0.5 h / Heating
6: 1.) Na / 1.) ethanol; 2.) ethanol, reflux
7: H2O, KOH / Heating
8: 94.6 percent / quinoline / 0.33 h / Heating
9: 95 percent / cc. H2SO4 / toluene
10: 99 percent / B2H6 / tetrahydrofuran
11: 86 percent / 48 percent HBr / H2O / 0.5 h / Heating
12: 1.) Na / 1.) ethanol; 2.) ethanol, reflux
13: H2O, KOH / Heating
14: diethylformamide / Heating
15: SOCl2 / Heating
With
quinoline; potassium hydroxide; thionyl chloride; N-ethylpropionamide; sulfuric acid; water; hydrogen bromide; sodium; diborane;
In
tetrahydrofuran; water; toluene;
- Guidance literature:
-
Multi-step reaction with 11 steps
1: 91.2 percent / 48 percent HBr / H2O / 0.5 h / Heating
2: 1.) Na / 1.) ethanol; 2.) ethanol, reflux
3: H2O, KOH / Heating
4: 94.6 percent / quinoline / 0.33 h / Heating
5: 95 percent / cc. H2SO4 / toluene
6: 99 percent / B2H6 / tetrahydrofuran
7: 86 percent / 48 percent HBr / H2O / 0.5 h / Heating
8: 1.) Na / 1.) ethanol; 2.) ethanol, reflux
9: H2O, KOH / Heating
10: diethylformamide / Heating
11: SOCl2 / Heating
With
quinoline; potassium hydroxide; thionyl chloride; N-ethylpropionamide; sulfuric acid; water; hydrogen bromide; sodium; diborane;
In
tetrahydrofuran; water; toluene;