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
CONDITIONS
反应条件
- 温度
- -70 °C
PROCEDURE
实验过程
To a solution of 312 mg (7.82 mmol) of sodium hydride (60% oil dispersion) in 10 mL of N,N-dimethylformamide was added 1.43 g (7.82 mmol) of ethyl-3-amino-4,4,4-trifluorocrotonate in 7 mL of toluene over a period of 30 min at -5° C. The resulting mixture was stirred for an additional 30 min before it was cooled to -70° C. Then a solution of 2.17 g (7.82 mmol) of 4-chloro-2-fluoro-5-(phenylmethoxy)phenyl isocyanate in 7 mL of toluene was added dropwise at a rate that maintained the reaction temperature below -60° C. After the addition, the thick reaction mixture was maintained at -60° C. for an additional 1 h before the cooling bath was removed. The mixture was gradually warmed to room temperature and stirring was continued for 1.5 h. Then the mixture was poured into a solution of 10 mL of concentrated HCl in 200 mL of water. The toluene layer was separated and the aqueous layer was further extracted twice with 200 mL of ether, dried (MgSO4), concentrated in vacuo to give yellow oil which was flash chromatographed over silica gel eluting with a 1:4 v:v mixture of ethyl acetate and hexane to give 1.85 g of the title compound as a pale yellow foam: 1H-NMR (CDCl3, 200 MHz): ppm 7.40 (m, 6H), 6.85 (d, 1H), 6.2 (s, 1H), 5.05 (s, 2H).
WORKUP
后处理
- temperaturemaintained the reaction temperature below -60° C
- additionAfter the addition
- temperaturethe thick reaction mixture was maintained at -60° C. for an additional 1 h before the cooling bath
- customwas removed
- temperatureThe mixture was gradually warmed to room temperature
- stirringstirring
- waitwas continued for 1.5 h
- additionThen the mixture was poured into a solution of 10 mL of concentrated HCl in 200 mL of water
- customThe toluene layer was separated
- extractionthe aqueous layer was further extracted twice with 200 mL of ether
- dry with materialdried (MgSO4)
- concentrationconcentrated in vacuo
- customto give yellow oil which
- customchromatographed over silica gel eluting with a 1:4 v
- additionv mixture of ethyl acetate and hexane