Technology Process of Cyclohexaneacetic acid, 4-[4-(broMoMethyl)phenyl]-, ethyl ester, trans-
There total 7 articles about Cyclohexaneacetic acid, 4-[4-(broMoMethyl)phenyl]-, ethyl ester, trans- 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
hydrogen bromide; acetic acid;
In
water;
for 1.5h;
Inert atmosphere;
DOI:10.1021/jm201524g
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: aluminum (III) chloride / n-heptane; dichloromethane / 0.75 h / -5 - 10 °C / Inert atmosphere
1.2: 0.5 h / -5 - 20 °C / Inert atmosphere
2.1: 5%-palladium/activated carbon; hydrogen; triethylamine / tetrahydrofuran / 18 h / 20 °C / 2068.65 Torr
3.1: hydrogen bromide; acetic acid / water / 1.5 h / Inert atmosphere
With
aluminum (III) chloride; 5%-palladium/activated carbon; hydrogen bromide; hydrogen; acetic acid; triethylamine;
In
tetrahydrofuran; n-heptane; dichloromethane; water;
DOI:10.1021/jm201524g
- Guidance literature:
-
Multi-step reaction with 2 steps
1: 5%-palladium/activated carbon; hydrogen; triethylamine / tetrahydrofuran / 18 h / 20 °C / 2068.65 Torr
2: hydrogen bromide; acetic acid / water / 1.5 h / Inert atmosphere
With
5%-palladium/activated carbon; hydrogen bromide; hydrogen; acetic acid; triethylamine;
In
tetrahydrofuran; water;
DOI:10.1021/jm201524g
