General and efficient palladium-catalyzed aminations of aryl chlorides
โ Scribed by Xiaohong Bei; Anil S. Guram; Howard W. Turner; W.Henry Weinberg
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 191 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
Pd(dba)~fl_~igand A catalyst efficiently catalyzes the aminations of a variety of aryl chlorides with a variety of amines in high rates, selectivities, and isolated yields.
๐ SIMILAR VOLUMES
## The palladium-catalyzed coupling reaction of aryl chlorides with various amines has been studied for the first time. Crucial for the success of this C-N bond forming reaction is the use of potassium tertbutoxide as base. Turn over numbers up to 900 and yields up to 80 % have been obtained.
Pd(PCy3)CI 2 (Cy = cyclohexyi) catalyzed the rcactioa of aryl cldmides and ~,,octdary amln~ in the pre~ncยข of NaOtBu to give the ~g aryl amines in good to excellent yields. In of dte reactions, an excess amouat of aryl chloride (atyl chloride/amine = 2) improved the yields.
Palladium-Catalyzed Reactions for Fine Chemical Synthesis. Part 2. First Palladium-Catalyzed Aminations of Aryl Chlorides. -The use of KO-tBu as base is found to be crucial for the success of the title amination.