反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
Ethyl 4,4,4-trifluorobutyrate (1 g, 5.88 mmol) and diethyl oxalate (3.87 g, 26.5 mmol) was dissolved in ethanol. Sodium ethoxide (21% in ethanol, 2.09 g) was added to the solution, and the reaction mixture stirred for 0.5 hrs. Solvent was distilled, and the residue extracted with EtOAc/water. The organic layers were collected and dried over sodium sulfate. After filtration, solvent was removed to give a clear liquid. MS (ESI): m/z 269.1 (M−1). The liquid was then dissolved in 3N HCl (20 mL), and the reaction mixture refluxed for 4 hrs. After cooling down, the reaction mixture was extracted with EtOAc. The organic layers were collected and dried over sodium sulfate. After filtration, solvent was removed, and the residue used directly in the next step. MS (ESI): m/z 169.7 (M−1).
WORKUP
后处理
- distillationSolvent was distilled
- extractionthe residue extracted with EtOAc/water
- customThe organic layers were collected
- dry with materialdried over sodium sulfate
- filtrationAfter filtration, solvent
- customwas removed
- customto give a clear liquid
- temperaturethe reaction mixture refluxed for 4 hrs
- temperatureAfter cooling down
- extractionthe reaction mixture was extracted with EtOAc
- customThe organic layers were collected
- dry with materialdried over sodium sulfate
- filtrationAfter filtration, solvent
- customwas removed