Réaction #632025

Équation de réaction

ethyl 2-(5-oxo-6,7,8,9-tetrahydro-5H-benzo[7]annulen-6-yl)acetate

potassium hydroxide

→

2-(5-oxo-6,7,8,9-tetrahydro-5H-benzo[7]annulen-6-yl)acetic acid

Solvants

ethanol

Conditions de réaction

Traitement

1. 1
   Températurethe resulting mixture was refluxed for 2 h
2. 2
   Autrethe EtOH was removed by evaporation
3. 3
   ExtractionThe residue was extracted with EtOAc twice (15 mL×2)
4. 4
   AutreThe aqueous layer was then transferred into a flask
5. 5
   Températurecooled with an ice-water bath
6. 6
   workup.ADDITIONHCl was added dropwise
7. 7
   workup.ADDITIONEtOAc (60 mL) was then added
8. 8
   Autrethe layers were separated
9. 9
   Extractionthe aqueous layer was extracted with EtOAc
10. 10
    LavageThe combined extracts were washed with brine
11. 11
    SéchageAfter being dried (MgSO4)
12. 12
    Filtrationfiltered
13. 13
    Concentrationconcentrated

Mode opératoire

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+).

Source