Реакция #80724
ord-cc3be286e8cd48f59b1ed630a6448864
Уравнение реакции
4,4-dimethyl-2-oxo-1,2,3,4-tetrahydro-6-[(trimethylsilyl)ethynyl]quinoline
4,4-dimethyl-2-oxo-1,2,3,4-tetrahydro-6[(trimethylsilyl)ethynyl]quinoline
Compound 2
4,4-dimethyl-2-oxo-1,2,3,4-tetrahydro-6[(trimethylsilyl)ethynyl]quinoline
4,4-dimethyl-2-oxo-1,2,3,4-tetrahydro-7-bromoquinoline
Compound 18
4,4-dimethyl-2-oxo-1,2,3,4-tetrahydro-7-bromoquinoline
triethylamine
→
Реактанты
4,4-dimethyl-2-oxo-1,2,3,4-tetrahydro-6-[(trimethylsilyl)ethynyl]quinoline
4,4-dimethyl-2-oxo-1,2,3,4-tetrahydro-6[(trimethylsilyl)ethynyl]quinoline
Compound 2
4,4-dimethyl-2-oxo-1,2,3,4-tetrahydro-6[(trimethylsilyl)ethynyl]quinoline
—
trimethylacetylene
4,4-dimethyl-2-oxo-1,2,3,4-tetrahydro-7-bromoquinoline
Compound 18
4,4-dimethyl-2-oxo-1,2,3,4-tetrahydro-7-bromoquinoline
triethylamine
Реагенты
Условия реакции
Подробные условия
See reaction.notes.procedure_details.
Методика
2.2398 g (8.8 mmol) of 4,4-dimethyl-2-oxo-1,2,3,4-tetrahydro-7-bromoquinoline (Compound 18), 371 mg (1.9 mmol) of CuI, 1.087 g (1.5 mmol) of Pd(PPh3)2Cl2, 35 ml (0.251 mol) of triethylamine and 4.0 ml (28.0 mmol) of trimethylacetylene were reacted substantially in accordance with the procedure used for the preparation of 4,4-dimethyl-2-oxo-1,2,3,4-tetrahydro-6-[(trimethylsilyl)ethynyl]quinoline (Compound 2) to give the title compound as pale orange solids (74%).