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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1076341Generated: October 31, 2026

Acetic Acid → HCID 54172588, compound

https://huagongshe.com/reaction/1076341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantBenzeneHCID 241—
ReactantIodineHCID 807—
ReactantMethyl bromoacetateHCID 60984—
ReactantHCID 22457011HCID 22457011—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
ProductHCID 54172588HCID 54172588—

Reaction Steps

A solution of 13.0 g. of 6-cyano-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 3 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 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-5-cyano-indenyl)acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03956363
Source datasetuspto-grants-1976_05
ORD IDord-c7d441d4b8d64926895fcf2b36203d90
Source noteuspto-grants-1976_05