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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1939355Generated: October 30, 2026

Ethanol → HCID 54003979, compound

https://huagongshe.com/reaction/1939355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantIodineHCID 807—
ReactantMethyl bromoacetateHCID 60984—
Reactant6-Methoxy-2-methyl-2,3-dihydro-1H-inden-1-oneHCID 231178—
SolventAcetic AcidHCID 176—
SolventBenzeneHCID 241—
SolventDiethyl EtherHCID 3283—
ProductHCID 54003979HCID 54003979—

Reaction Steps

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. Coil., 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 h. After addition of 30 ml of 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-indanyl)acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05696159
Source datasetuspto-grants-1997_12
ORD IDord-5e28f59e3d7e480bb0a28c7c27fab3c7
Source noteuspto-grants-1997_12