HRID220455
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
- -78 °C
PROCEDURE
实验过程
Dissolve 4-bromo-1,5-dimethyl-3-trifluoromethyl-1H-pyrazole (0.30 g, 1.23 mmol) in tetrahydrofuran (14.7 mL). Cool to −78° C. and add 1.7 M t-butyllithium in pentane (2.9 mL) dropwise. Stir for 3 min. at −78° C. and then add dimethylformamide (669 μL, 8.64 mmol). Stir for thirty min. at −78° C., then warm to 0° C. over 2 hr. Add 2 N hydrochloric acid (12.3 mL) and stir at room temperature for one hr. Separate layers and extract aqueous layer 2 times with DCM. Dry combined organic layers (magnesium sulfate), filter, concentrate and purify (silica gel chromatography eluting with 0:100 to 15:85 ethyl acetate:hexanes), to give the title preparation (79 mg, 33%). GC-MS: m/z=192 [M+].
WORKUP
后处理
- stirringStir for thirty min. at −78° C.
- temperaturewarm to 0° C. over 2 hr
- stirringstir at room temperature for one hr
- extractionSeparate layers and extract aqueous layer 2 times with DCM
- customDry
- filtrationfilter
- concentrationconcentrate
- custompurify
- wash(silica gel chromatography eluting with 0:100 to 15:85 ethyl acetate:hexanes)
- customto give the title
- custompreparation (79 mg, 33%)