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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1017290Generated: October 27, 2026

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

https://huagongshe.com/reaction/1017290

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantIodineHCID 807—
ReactantEthyl bromoacetateHCID 7748—
Reactant6-Methoxy-2-methyl-2,3-dihydro-1H-inden-1-oneHCID 231178—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
ProductEthyl-(1-hydroxy-2-methyl-6-methoxy-indenyl) acetateHCID 57181931—

Reaction Steps

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 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 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.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06479493B1
Source datasetuspto-grants-2002_11
ORD IDord-08e32a710ddf4634942b7035e7bbdcca
Source noteuspto-grants-2002_11