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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1077141Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1077141

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
PatentnummerUS03959322
Quelldatensatzuspto-grants-1976_05
ORD IDord-8782780bea62495b8605cb452e75635c
Quellennotizuspto-grants-1976_05