HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
4-Formylbenzoic acid → 4-[3-Oxo-3-(7,8-dihydro-5-(2-thienyl)-8,8-dimethyl-2-naphthalenyl)-1-propenyl)-benzoic acid
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 4-Formylbenzoic acid | HCID 12088 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 3,4-Dihydro-1-(2-thienyl)-4,4-dimethyl-6-acetylnaphthalene | HCID 22571541 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | 4-[3-Oxo-3-(7,8-dihydro-5-(2-thienyl)-8,8-dimethyl-2-naphthalenyl)-1-propenyl)-benzoic acid | HCID 54528150 | — |
Reaktionsschritte
To a solution of 62.6-mg (0.222 mmol) 3,4-dihydro-1-(2-thienyl)-4,4-dimethyl-6-acetylnaphthalene (Compound D33) in 4.0 mL of MeOH were added 33.4 mg (0.222 mmol) of 4-carboxy benzaldehyde, and 240.0 mg (6.00 mmol; 2.0 mL of 3M aqueous NaOH). The resulting solution was stirred at room temperature for 12 h, concentrated under reduced pressure, and the residual oil dissolved in EtOAc. The solution was treated with 10% HCl, and the organic layer washed with H2O, and saturated aqueous NaCl, before being dried over Na2SO4. Removal of the solvents under reduced pressure gave the title compound as a pale green solid after recrystallization from EtOH.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06855832B2 |
| Quelldatensatz | uspto-grants-2005_02 |
| ORD ID | ord-1313fb2a46c74e41ba43a2712ec20dc4 |
| Quellennotiz | uspto-grants-2005_02 |