Reacción #684947
ord-63e429487d474d50b8f9c5f09af3289a
Ecuación de reacción
Reactantes
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1Concentraciónthis was concentrated
- 2workup.ADDITIONtoluene and water were added to this residue
- 3LavadoThe toluene layer was washed with water
- 4Secadodried over potassium carbonate
- 5Concentraciónconcentrated
- 6workup.ADDITIONTo an ethanol (1.6 ml) solution of the residue, 50% aqueous sodium hydroxide solution (0.63 ml) was added
- 7Temperaturathis was refluxed for 2 hours
- 8ConcentraciónAfter concentration, toluene and water
- 9workup.ADDITIONwere added
- 10LavadoThe toluene layer was washed with water
- 11Secadodried over calcium carbonate
- 12Concentraciónconcentrated
- 13OtroThe residue was purified by silica gel column chromatography
Procedimiento
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).