HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Methanol → 2-(6-m-Acetoxyphenyl-3-oxohexyl)-2-methylcyclopentane-1,3-dione
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Methanol | HCID 887 | — |
| Edukt | 2-Methyl-1,3-cyclopentanedione | HCID 13005 | — |
| Edukt | 6-m-Acetoxyphenyl-1-diethylaminohexan-3-one | HCID 21485420 | — |
| Edukt | 6-m-Acetoxyphenylhex-1-en-3-one | HCID 21485580 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Lösungsmittel | Potassium Hydroxide | HCID 14797 | — |
| Produkt | 2-(6-m-Acetoxyphenyl-3-oxohexyl)-2-methylcyclopentane-1,3-dione | HCID 21485772 | — |
Reaktionsschritte
Reflux a mixture of 6-(m-acetoxyphenyl)-1-diethylaminohexan-3-one and 6-(m-acetoxyphenyl)hex-1-en-3-one (1 g), with 2-methylcyclopentane-1,3-dione (1.5 g) in 0.12% methanolic potassium hydroxide (6 cc) for 18 hours. Remove methanol (2 cc) under reduced pressure and add chloroform (60 cc). Wash the solution in turn with dilute sulfuric acid (25 cc), saturated potassium bicarbonate solution, and brine; dry and evaporate the solvent. The product (0.8 g) is the adduct 2-(6-m-acetoxyphenyl-3-oxohexyl)-2-methylcyclopentane-1,3-dione in admixture with some of the corresponding free phenol; infrared absorption: 2.86 to 3.08 (broad low-intensity band), 5.71, 5.81, 5.85, and 8.26 μ.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US03959322 |
| Quelldatensatz | uspto-grants-1976_05 |
| ORD ID | ord-8782780bea62495b8605cb452e75635c |
| Quellennotiz | uspto-grants-1976_05 |