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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1414958Erstellt: 27. Oktober 2026

Methanol → 2-(6-m-Acetoxyphenyl-3-oxohexyl)-2-methylcyclopentane-1,3-dione

https://huagongshe.com/reaction/1414958

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
Edukt2-Methyl-1,3-cyclopentanedioneHCID 13005—
Edukt6-m-Acetoxyphenyl-1-diethylaminohexan-3-oneHCID 21485420—
Edukt6-m-Acetoxyphenylhex-1-en-3-oneHCID 21485580—
LösungsmittelChloroformHCID 6212—
LösungsmittelPotassium HydroxideHCID 14797—
Produkt2-(6-m-Acetoxyphenyl-3-oxohexyl)-2-methylcyclopentane-1,3-dioneHCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04002746
Quelldatensatzuspto-grants-1977_01
ORD IDord-bd5a066270e1404bb3a2ccbce35d50b6
Quellennotizuspto-grants-1977_01