Technology Process of C28H21FN2O2
There total 5 articles about C28H21FN2O2 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
palladium diacetate; sodium t-butanolate; XPhos;
In
toluene; tert-butyl alcohol;
at 90 ℃;
Inert atmosphere;
DOI:10.1021/jm300951u
- Guidance literature:
-
Multi-step reaction with 3 steps
1: oxalyl dichloride; N,N-dimethyl-formamide / dichloromethane / 1 h / 20 °C / Inert atmosphere
2: aluminum (III) chloride / dichloromethane / 4 h / 20 °C
3: palladium diacetate; XPhos; sodium t-butanolate / tert-butyl alcohol; toluene / 90 °C / Inert atmosphere
With
aluminum (III) chloride; oxalyl dichloride; palladium diacetate; N,N-dimethyl-formamide; sodium t-butanolate; XPhos;
In
dichloromethane; toluene; tert-butyl alcohol;
2: |Friedel-Crafts Acylation / 3: |Buchwald-Hartwig Coupling;
DOI:10.1021/jm300951u
- Guidance literature:
-
Multi-step reaction with 2 steps
1: aluminum (III) chloride / dichloromethane / 4 h / 20 °C
2: palladium diacetate; XPhos; sodium t-butanolate / tert-butyl alcohol; toluene / 90 °C / Inert atmosphere
With
aluminum (III) chloride; palladium diacetate; sodium t-butanolate; XPhos;
In
dichloromethane; toluene; tert-butyl alcohol;
1: |Friedel-Crafts Acylation / 2: |Buchwald-Hartwig Coupling;
DOI:10.1021/jm300951u