HRID1348651
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
A solution of 3.00 g (10.0 mmol) ((6R,7S)-2-fluoro-6-methyl-8-oxo-6,7,8,9-tetrahydro-5-oxa-9-aza-benzocyclohepten-7-yl)-carbamic acid tert-butyl ester and 3.37 g (15.0 mmol) 2,2,2-trifluoroethyl triflate in 30 ml dimethylformamide were treated with 4.73 g (15.0 mmol) cesium carbonate for 6 hours. The solvent was distilled off at low pressure and the residue was extracted with water/ethylacetate. Chromatography on silicagel with heptane/ethylacetate 100:0 to 0:100 yielded 3.79 g (99%) [(6R,7S)-2-fluoro-6-methyl-8-oxo-9-(2,2,2-trifluoro-ethyl)-6,7,8,9-tetrahydro-5-oxa-9-aza-benzocyclohepten-7-yl]-carbamic acid tert-butyl ester, MS m/e (%): 393.3 (M+H+, 100).
WORKUP
后处理
- distillationThe solvent was distilled off at low pressure
- extractionthe residue was extracted with water/ethylacetate