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CAS RN: 5439-14-5 | 产品编码: D1393
3,4-Dihydro-2H-pyrido[1,2-a]pyrimidin-2-one
![3,4-Dihydro-2H-pyrido[1,2-a]pyrimidin-2-one Chemical Structure of 3,4-Dihydro-2H-pyrido[1,2-a]pyrimidin-2-one](/medias/D1393.jpg?context=bWFzdGVyfHJvb3R8NDg1NzJ8aW1hZ2UvanBlZ3xhREV3TDJoaU15ODRPVEl4TURReU9URXhNall5TDBReE16a3pMbXB3Wnd8ZGM4NDMxN2I0ZTU5N2VjODU1MzUzYWE4MjIwZDNiYWY1ZjQwNzBjODFjOTRiMmE3YjM3YjFiYzMyZGE3OWMwMQ)
技术规格
Appearance | White to Almost white powder to crystal |
Purity(HPLC) | min. 98.0 area% |
Purity(Nonaqueous Titration) | min. 98.0 % |
NMR | confirm to structure |
物性(参考值)
GHS
相关法规
运输信息
HS编码* | 2933.99-000 |
应用
An Effective Acid Captor of Mukaiyama Condensation Reaction
Experimental procedure: To a mixture of 2-fluoro-1-methylpyridinium p-toluenesulfonate (1.2 mmol) and 3,4-Dihydro-2H-pyrido[1,2-a]pyrimidin-2-one (4.8 mmol) is added a dichloromethane solution (4 mL) of pentanoic acid (1.0 mmol) and benzyl alcohol (1.0 mmol) at room temperature under argon atmosphere, and the resulting mixture is stirred at room temperature for 46 h. After evaporation of the solvent under reduced pressure, the residue is chromatographed on silica gel, and benzyl pentanoate is isolated (74% yield).
References
- BETAINE AS AN EFFECTIVE ACID CAPTOR: A CONVENIENT METHOD FOR THE SYNTHESIS OF CARBOXYLIC ESTERS
参考文献