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 7.3 g 4-Bromo-1H-indole-2-carboxylic acid tert-butyl ester in 100 ml DMF, 6.8 ml NEt3, 276 mg Pd(OAc)2, 128 mg 1,1′-Bis(diphenylphosphino)ferrocene, 12 ml MeOH were added and purged with argon for 15 min. This solution was then purged with carbon monoxide and heated to 70° C. for 4 h. The reaction mixture was concentrated under reduced pressure, the residue dissolved in 200 ml DCM and washed with 100 ml water. The organic layer was dried over MgSO4 and, after removal of the solvent under reduced pressure, the residue was purified by chromatography on silica gel eluting with n-heptane/ethyl acetate 9:1. The fractions containing the product were collected and concentrated under reduced pressure. Yield: 3.8 g. MS (ESI+): m/e=276.
WORKUP
后处理
- custompurged with argon for 15 min
- customThis solution was then purged with carbon monoxide
- concentrationThe reaction mixture was concentrated under reduced pressure
- dissolutionthe residue dissolved in 200 ml DCM
- washwashed with 100 ml water
- dry with materialThe organic layer was dried over MgSO4
- customafter removal of the solvent under reduced pressure
- customthe residue was purified by chromatography on silica gel eluting with n-heptane/ethyl acetate 9:1
- additionThe fractions containing the product
- customwere collected
- concentrationconcentrated under reduced pressure