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
PdCl2 (35.5 mg, 0.2 mmol) and the sodium salt of trisulfonated triphenylphosphine (TPPTS) [1.136 g, 2 mmol, P/Pd=10] are charged into a tube under argon. To the mixture is added 50 g of deairated distilled H2O. After 25 minutes of stirring at room temperature, the PdCl2 is completely dissolved and the mixture becomes bright yellow, indicating complexation of palladium (II) with TPPTS (pH of the solution=3.42). The catalyst solution, 1-(4-isobutyl-phenyl)ethanol (IBPE) [445.7 mg, 2.5 mmol, IBPE/Pd=12.5], p-toluenesulfonic acid monohydrate (190.2 rag, 1 mmol, H+ /IBPE=0.4) and deairated distilled H2O (90.4 g, [Pd]=150 ppm in the aqueous solution) are charged into a 300 ml Hastelloy C autoclave under argon. After a number of pressurizing-depressurizing cycles with CO to remove the last air, the autoclave is pressured to 30 bar (final pressure at reaction temperature) and contents are heated to 90° C. for 20 hours with stirring. The autoclave is cooled to room temperature, CO vented, and the reaction mixture is removed. Alter extraction with diethylether, the organic layer is separated from the aqueous layer (pH=2.21) and is dried over magnesium sulfate. The organic fraction, alter concentration under reduced pressure, is analyzed by HPLC and contains IBPE, 2-(4-isobutyl-phenyl)propionic acid (ibuprofen), 3-(4-isobutylphenyl)propionic acid (3-IPPA) which is a linear isomer of ibuprofen and traces of 4-isobutylstyrene. Conversion (based on IBPE) is 49%. Selectivity of ibuprofen is 61.5%. Selectivity of 3-IPPA is 38.3%.
WORKUP
后处理
- additionTo the mixture is added 50 g
- distillationof deairated distilled H2O
- dissolutionthe PdCl2 is completely dissolved
- customAfter a number of pressurizing-depressurizing cycles with CO to remove the last air
- customat reaction temperature) and contents
- temperatureare heated to 90° C. for 20 hours
- stirringwith stirring
- temperatureThe autoclave is cooled to room temperature
- customthe reaction mixture is removed
- extractionAlter extraction with diethylether
- customthe organic layer is separated from the aqueous layer (pH=2.21)
- dry with materialis dried over magnesium sulfate
- concentrationconcentration under reduced pressure