Technology Process of 2-Benzyl-2H-dibenzisoindol
There total 4 articles about 2-Benzyl-2H-dibenzisoindol 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
acetic anhydride; triethylamine;
In
chloroform;
1.) 15 min, 0 deg C, 2.) 3.5h, r.t.;
- Guidance literature:
-
Multi-step reaction with 4 steps
1: N-bromosuccinimide, azobis isobutyronitrile
2: 76 percent / ethyl diisopropylamine / CH2Cl2 / 5 h / Heating
3: 78 percent / 60percent H2O2 / methanol; CHCl3 / 72 h / Ambient temperature; 1.) 3d, r.t., 2.) 1d, r.t.
4: 68 percent / Et3N, acetic anhydride / CHCl3 / 1.) 15 min, 0 deg C, 2.) 3.5h, r.t.
With
N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); dihydrogen peroxide; acetic anhydride; triethylamine; N-ethyl-N,N-diisopropylamine;
In
methanol; dichloromethane; chloroform;
- Guidance literature:
-
Multi-step reaction with 3 steps
1: 76 percent / ethyl diisopropylamine / CH2Cl2 / 5 h / Heating
2: 78 percent / 60percent H2O2 / methanol; CHCl3 / 72 h / Ambient temperature; 1.) 3d, r.t., 2.) 1d, r.t.
3: 68 percent / Et3N, acetic anhydride / CHCl3 / 1.) 15 min, 0 deg C, 2.) 3.5h, r.t.
With
dihydrogen peroxide; acetic anhydride; triethylamine; N-ethyl-N,N-diisopropylamine;
In
methanol; dichloromethane; chloroform;