| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5266032 | Tetrahedron Letters | 2011 | 4 Pages |
Abstract
N-heterocyclic carbene (NHC) has been employed as an efficient catalyst for cyanation reaction of carbonyl compounds. Under catalysis of 1 mol % NHCs, various aldehydes and 2,2,2-trifluoroacetophenone coupled with ethyl cyanoformate in THF to provide cyanohydrins ethyl carbonates in excellent yields. While in the presence of 10 mol % catalyst, different types of aldehydes and 2,2,2-trifluoroacetophenone reacted with acetyl cyanide in dichloroethane to give acylated cyanohydrins in moderate to high yields.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Jie Zhang, GuangFen Du, YueKe Xu, Lin He, Bin Dai,
