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
- 100 °C
PROCEDURE
实验过程
A mixture of 4-bromo-1-fluoro-2-nitrobenzene 324 mg, ethyl 3-(1H-imidazol-2-yl)propanoate 248 mg, potassium carbonate 407 mg and N,N-dimethylacetamide 10 mL was heated at 100° C. for 12 hours in nitrogen atmosphere. The reaction liquid was diluted with ethyl acetate and water was added thereto to induce phase separation. The organic layer was washed with saturated brine and dried over sodium sulfate, from which then the solvent was distilled off. Thus obtained oily substance was dissolved in a liquid mixture of 10 mL of acetic acid and 10 mL of water, and to the solution 1.51 g of 85% sodium hydrosulfite was added, followed by 2 hours' heating under reflux. The reaction liquid was cooled with ice and neutralized with saturated aqueous sodium hydrogencarbonate solution. Extracting the same with ethyl acetate, the extract was washed with saturated brine, dried over sodium sulfate, and from which the solvent was distilled off. To the resulting oily substance, 358 mg of 1,1′-carbonyldiimidazole and 20 mL of 1,2-dichlorobenzene were added, followed by 5 hours' heating under reflux in nitrogen atmosphere. The solvent was distilled off, and to the residue methanol was added and stirred overnight. Thus precipitated crystals were recovered by filtration, washed with methanol and dried in flowing air to provide 112 mg of the title compound.
WORKUP
后处理
- customThe reaction liquid
- additionwas added
- customphase separation
- washThe organic layer was washed with saturated brine
- dry with materialdried over sodium sulfate, from which
- distillationthe solvent was distilled off
- dissolutionThus obtained oily substance was dissolved in a liquid mixture of 10 mL of acetic acid and 10 mL of water
- additionto the solution 1.51 g of 85% sodium hydrosulfite was added
- temperature' heating
- temperatureunder reflux
- customThe reaction liquid
- extractionExtracting the same with ethyl acetate
- washthe extract was washed with saturated brine
- dry with materialdried over sodium sulfate
- distillationfrom which the solvent was distilled off
- additionTo the resulting oily substance, 358 mg of 1,1′-carbonyldiimidazole and 20 mL of 1,2-dichlorobenzene were added
- waitfollowed by 5 hours
- temperature' heating
- temperatureunder reflux in nitrogen atmosphere
- distillationThe solvent was distilled off
- additionto the residue methanol was added
- filtrationThus precipitated crystals were recovered by filtration
- washwashed with methanol
- customdried