Reacción #409098
ord-170e1cf225264e478a69db13dd9afd18
Ecuación de reacción
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1workup.ADDITIONwas added slowly
- 2TemperaturaThe dark brown reaction mixture was cooled to 30° C.
- 3workup.STIRRINGvigorously stirred in a cooling bath
- 4ExtracciónThe resulting mixture was then extracted with Et2O (5×200 mL)
- 5LavadoThe combined organic layers were washed successively with water, saturated sodium bicarbonate solution and water
- 6ExtracciónThe washed organic extract
- 7Secadowas then dried over anhydrous MgSO4
- 8Concentraciónconcentrated in vacuo
- 9workup.DISTILLATIONThe residue was distilled at 130-135° C. at 4 mmHg
- 10Otroto yield 3.5 g, 25%, about 90% purity
- 11OtroThis product was chromatographed on silica gel
Procedimiento
A stirred suspension of 1-cyclopentene carboxylic acid (11.2 g, 100 mmol) and cyclopentene (13.6 g, 200 mmol) was added slowly to stirring polyphosphoric acid (Aldrich, 300 g) at 60° C. in a 250 mL flask. The reaction mixture was stirred at 70-80° C. for 4 hours under nitrogen. The dark brown reaction mixture was cooled to 30° C. and poured on 300 g of ice and vigorously stirred in a cooling bath. The brown mass was then neutralized with a saturated solution of ammonium sulfate (200 ml). The resulting mixture was then extracted with Et2O (5×200 mL). The combined organic layers were washed successively with water, saturated sodium bicarbonate solution and water. The washed organic extract was then dried over anhydrous MgSO4 and concentrated in vacuo. The residue was distilled at 130-135° C. at 4 mmHg to yield 3.5 g, 25%, about 90% purity. This product was chromatographed on silica gel using hexane and ethyl acetate as eluent to obtain pure cis-tricyclo[6.3.0.03,7]undec-1(8)-en-2-one. 1H-NMR (CDCl3): δ3.2 (m, 1 H), 3.1 (m, 1H), 2.5 (m, 2H), 2.4 (m, 4H), 1.9 (m, 1H), 1.6 (m, 4H), 1.3 (m, 1H).