Mechanism of the formation of N,N-dialkyl-2-pyrrolecarboxamides from 1,3-diketones and N,N-dialkyloximinoacetoacetamides
✍ Scribed by Paine, John B.; Brough, Jonathan R.; Buller, Kathy K.; Erikson, Erika E.; Dolphin, David
- Book ID
- 118156429
- Publisher
- American Chemical Society
- Year
- 1987
- Tongue
- English
- Weight
- 681 KB
- Volume
- 52
- Category
- Article
- ISSN
- 0022-3263
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📜 SIMILAR VOLUMES
## Abstract A recently discovered method for the synthesis of __N,N__‐dialkyl‐1,3‐benzenediamines with two different alkyl groups is shown to be general. This is demonstrated by the synthesis of __N__‐butyl‐__N__‐phenethyl‐1,3‐benzenediamine by the condensation of 3‐nitroaniline with phenyl‐acetald
A mild, convenient, and practical one-pot procedure for direct synthesis of N,N 0 -dialkyl-N 00 -dialkylaminocarbothioyl thioureas is described via three-component reaction of cyclic secondary amines, CS 2 , and N,N 0 -dialkyl carbodiimides in water at room temperature.