Reacción #632025
ord-766af532e8c94ca7873ac840912c86b5
Ecuación de reacción
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1Temperaturathe resulting mixture was refluxed for 2 h
- 2Otrothe EtOH was removed by evaporation
- 3ExtracciónThe residue was extracted with EtOAc twice (15 mL×2)
- 4OtroThe aqueous layer was then transferred into a flask
- 5Temperaturacooled with an ice-water bath
- 6workup.ADDITIONHCl was added dropwise
- 7workup.ADDITIONEtOAc (60 mL) was then added
- 8Otrothe layers were separated
- 9Extracciónthe aqueous layer was extracted with EtOAc
- 10LavadoThe combined extracts were washed with brine
- 11SecadoAfter being dried (MgSO4)
- 12Filtraciónfiltered
- 13Concentraciónconcentrated
Procedimiento
The compound of formula (Db), ethyl 2-(5-oxo-6,7,8,9-tetrahydro-5H-benzo[7]annulen-6-yl)acetate, (6.6 g, 26.8 mmol) was dissolved in ethanol (EtOH) (30 mL), then 10% potassium hydroxide (KOH) aqueous solution (37.5 mL, 67 mmol) was added and the resulting mixture was refluxed for 2 h. After cooling to ambient temperature, the EtOH was removed by evaporation. The residue was extracted with EtOAc twice (15 mL×2). The aqueous layer was then transferred into a flask and cooled with an ice-water bath, con. HCl was added dropwise to adjust pH to about 2.0. EtOAc (60 mL) was then added, the layers were separated, and the aqueous layer was extracted with EtOAc. The combined extracts were washed with brine. After being dried (MgSO4), filtered, and concentrated, the compound of formula (Dc), 2-(5-oxo-6,7,8,9-tetrahydro-5H-benzo[7]annulen-6-yl)acetic acid, was obtained as an orange oil (5.7 g, 97%); 1H NMR (300 MHz, CDCl3) δ: 7.71-7.68 (m, 1H), 7.41-7.20 (m, 3H), 3.37-3.31 (m, 1H), 3.12-2.91 (m, 3H), 2.57-2.49 (m, 1H), 2.15-1.90 (m, 2H), 1.75-1.62 (m, 2H); LC-MS: purity: 100%; MS (m/e): 219 (MH+).