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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1704063Generated: October 30, 2026

Potassium Iodide → Methyl (5-indanyloxy)[p-(p-chlorophenoxy)phenyl]acetate

https://huagongshe.com/reaction/1704063

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant5-IndanolHCID 15118—
ReactantSodium MethoxideHCID 10942334—
ReactantMethyl alpha-Bromo-alpha-[p-(p-chlorophenoxy)phenyl]acetateHCID 20392594—
SolventBenzeneHCID 241—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductMethyl (5-indanyloxy)[p-(p-chlorophenoxy)phenyl]acetateHCID 12531866—

Reaction Steps

To a solution of 3.36 g of 5-indanol, 1.19 g of sodium methoxide and 50 mg of potassium iodide in 40 ml of methanol is added 7.11 g of methyl α-bromo-α-[p-(p-chlorophenoxy)phenyl]acetate in 10 ml of benzene. The mixture is refluxed overnight and added to 100 ml of water. The mixture is then extracted with 2 × 75 ml of ether and the combined extracts are washed with 50 ml of 5% NaOH, 50 ml of water, 50 ml of saturated brine and dried (MgSO4). Evaporation of the solvent yields a yellow oil. Chromatography on 100 g of silica gel (benzene, 400 ml) yields a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04125729
Source datasetuspto-grants-1978_11
ORD IDord-db082abda00d40c58822fc31e1c89ccd
Source noteuspto-grants-1978_11