Réaction #7645

Équation de réaction

ethyl chloro(oxo)acetate

2-[(cyclopentylcarbonyl)amino]butanoic acid

pyridine

→

Ethyl 3-[(cyclopentylcarbonyl)amino]-2-oxopentanoate

Solvants

tetrahydrofurane

Conditions de réaction

Traitement

1. 1
   Températureheated
2. 2
   TempératureWhile heating
3. 3
   Températureat reflux
4. 4
   TempératureThe reaction mixture is heated
5. 5
   Températureat reflux until no more evolution of gas
6. 6
   Extractionthe organic phase extracted with ethyl acetate
7. 7
   AutreThe dried organic phase is evaporated to dryness in vacuo
8. 8
   workup.DISSOLUTIONdissolved in ethanol
9. 9
   Autrethe solution directly used for the next reaction

Mode opératoire

1.6 g (8 mmol) 2-[(cyclopentylcarbonyl)amino]butanoic acid are suspended in 30 ml tetrahydrofurane and heated to reflux together with 1.91 g (24 mmol) pyridine and a bit of N,N-dimethylaminopyridine. While heating at reflux, 2.19 g (16 mmol) ethyl chloro(oxo)acetate are added dropwise. The reaction mixture is heated at reflux until no more evolution of gas can be observed. After cooling down to room temperature, the reaction mixture is added to ice water and the organic phase extracted with ethyl acetate. The dried organic phase is evaporated to dryness in vacuo, dissolved in ethanol and the solution directly used for the next reaction.

Source