Реакция #684947
ord-63e429487d474d50b8f9c5f09af3289a
Уравнение реакции
Реактанты
Реагенты
Растворители
Условия реакции
Обработка
- 1Концентрированиеthis was concentrated
- 2workup.ADDITIONtoluene and water were added to this residue
- 3ПромывкаThe toluene layer was washed with water
- 4Сушкаdried over potassium carbonate
- 5Концентрированиеconcentrated
- 6workup.ADDITIONTo an ethanol (1.6 ml) solution of the residue, 50% aqueous sodium hydroxide solution (0.63 ml) was added
- 7Температураthis was refluxed for 2 hours
- 8КонцентрированиеAfter concentration, toluene and water
- 9workup.ADDITIONwere added
- 10ПромывкаThe toluene layer was washed with water
- 11Сушкаdried over calcium carbonate
- 12Концентрированиеconcentrated
- 13ДругоеThe residue was purified by silica gel column chromatography
Методика
To a dimethylformamide (1.8 ml) solution of 60% sodium hydride (16 mg, 0.40 mmol), a dimethylformamide (3.6 ml) solution of 1-cyano-2-benzoyl-1,2-dihydroisoquinoline (100 mg, 0.38 mmol) synthesized according to the literature of Org. Synth., VI, 115 (1988), and 4-n-butylbenzylchloride (70 mg, 0.38 mmol) was added dropwise under nitrogen atmosphere at −16° C., and was further stirred at room temperature for 30 minutes. Water was added, this was concentrated, and toluene and water were added to this residue. The toluene layer was washed with water, dried over potassium carbonate, and concentrated. To an ethanol (1.6 ml) solution of the residue, 50% aqueous sodium hydroxide solution (0.63 ml) was added, and this was refluxed for 2 hours. After concentration, toluene and water were added. The toluene layer was washed with water, then dried over calcium carbonate, and then concentrated. The residue was purified by silica gel column chromatography to give 18 mg of the aforementioned compound of the formula (Ia).