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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 47636Erstellt: 24. Oktober 2026

Benzene → Ethyl-(1-hydroxy-2-methyl-6-methoxy-indenyl) acetate

https://huagongshe.com/de/reaction/47636

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzeneHCID 241—
EduktIodineHCID 807—
EduktEthyl bromoacetateHCID 7748—
Edukt6-Methoxy-2-methyl-2,3-dihydro-1H-inden-1-oneHCID 231178—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelEthanolHCID 702—
LösungsmittelDiethyl EtherHCID 3283—
ProduktEthyl-(1-hydroxy-2-methyl-6-methoxy-indenyl) acetateHCID 57181931—

Reaktionsschritte

A solution of 13.4 g of 6-methoxy-2-methylindanone and 21 g. of ethyl bromoacetate in 45 ml. benzene is added over a period of five minutes to 21 g. of zinc amalgam (prepared according to Org. Syn. Coll. Vol. 3) in 110 ml. benzene and 40 ml. dry ether. A few cyrstals of iodine are added to start the reaction, and the reaction mixture is maintained at reflux temperature (ca. 65°) with external heating. At three-hour intervals, two batches of 10 g. zinc amalgam and 10 g. bromoester are added and the mixture is then refluxed for 8 hours. After addition of 30 ml. of ethanol and 150 ml. of acetic acid, the mixture is poured into 700 ml. of 50% aqueous acetic acid. The organic layer is separated, and the aqueous layer is extracted twice with ether. The combined organic layers are washed thoroughly with water, ammonium hydroxide and water. Drying over sodium sulfate, evaporation of solvent in vacuo followed by pumping at 80° (bath temperature)(1-2 mm.) gives crude ethyl-(1-hydroxy-2-methyl-6-methoxy-indenyl) acetate (ca. 18 g.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06699894B1
Quelldatensatzuspto-grants-2004_03
ORD IDord-a6c73439dc694cfb8ef1cc2104f59d7f
Quellennotizuspto-grants-2004_03