## Abstract The oneβpot threeβstep process is based on the thermolysis of boron esters of hydroxyamides.
Synthesis of 2-oxazolines via boron esters of N-(2-hydroxyethyl) amides
β Scribed by Baris Ilkgul; Deniz Gunes; Okan Sirkecioglu; Niyazi Bicak
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- French
- Weight
- 271 KB
- Volume
- 51
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
A new, convenient, one-pot process is presented for the synthesis of 2-oxazolines in high yields (75-94%) via boron esters of N-(2-hydroxyethyl) amides. The procedure involves thermolysis of the boron esters at 240-260 Β°C, in the presence of solid CaO as an acid scavenger and allows the preparation of oxazolines from hydroxyethyl amides of aliphatic and aromatic monocarboxylic acids.
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Efficient Synthesis of 2-Methylaminothiazolines via Mitsunobu Reaction of N-(2-Hydroxyethyl)-N'-methyl-thioureas. -Easily available N-(2-hydroxyethyl)thioureas react under Mitsunobu conditions to yield iminothiazolidines. N-alkylated starting material gives under similar conditions a mixture of imi