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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 263615Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/263615

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzeneHCID 241—
EduktIodineHCID 807—
EduktMethyl bromoacetateHCID 60984—
Edukt6-Methoxy-2-methyl-2,3-dihydro-1H-inden-1-oneHCID 231178—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelEthanolHCID 702—
LösungsmittelDiethyl EtherHCID 3283—
ProduktMethyl(1-hydroxy-2-methyl-6-methoxy-indenyl)acetateHCID 131718936—

Reaktionsschritte

A solution of 13.4 g. of 6-methoxy-2-methylindanone and 19.3 g. of methyl bromoacetate in 45 ml. benzene is added over a period of 5 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 crystals 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 eight hours. After addition of 30 ml. ethanol and 150 ml. of acetic acid, the mixture is poured into 700 ml. of 1:1 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 temp.) (1-2 mm.) gives crude methyl(1-hydroxy-2-methyl-6-methoxy-indenyl)acetate.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05643959
Quelldatensatzuspto-grants-1997_07
ORD IDord-98c2847997d14e9399fc51afe34a057b
Quellennotizuspto-grants-1997_07