Реакция #418006
ord-cd3eb982504f451c9cdb4e6638c8c71d
Уравнение реакции
EtOAc
trimethylsilylacetylene
N-ethyl-2-(4-iodo-phenyl)-propionamide
→
desired product
N-Ethyl-2-(4-trimethylsilanylethynyl-phenyl)-propionamide
Реагенты
Растворители
Условия реакции
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1Промывкаthe organic layer is washed with saturated ammonium chloride solution and brine
- 2ДругоеThe organic layer is separated
- 3Сушкаdried over sodium sulphate
- 4Другоеthe solvent is evaporated
- 5ДругоеThe residue is purified by column chromatography (silicia gel; EtOAc/heptane, gradient 50% to 80%)
Методика
To 4.90 g (49.9 mmol) trimethylsilylacetylene in 450 mL acetonitrile are added 12.1 g (39.9 mmol) N-ethyl-2-(4-iodo-phenyl)-propionamide (IV.1) under argon, followed by 1.68 g (2.40 mmol) Pd(PPh3)2Cl2 as catalyst, 0.23 g (1.20 mmol) copper(I)iodide and 11.1 mL (80 mmol) TEA as base. The mixture is stirred at rt for 2.5 h. After that time, EtOAc is added and the organic layer is washed with saturated ammonium chloride solution and brine. The organic layer is separated, dried over sodium sulphate and the solvent is evaporated. The residue is purified by column chromatography (silicia gel; EtOAc/heptane, gradient 50% to 80%) to yield the desired product.