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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1863323Generated: November 1, 2026

Potassium Iodide → HCID 12531865, compound

https://huagongshe.com/reaction/1863323

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant5,6,7,8-Tetrahydro-1-naphtholHCID 68258—
ReactantSodium MethoxideHCID 10942334—
ReactantMethyl alpha-Bromo-alpha-[p-(p-chlorophenoxy)phenyl]acetateHCID 20392594—
SolventBenzeneHCID 241—
SolventMethanolHCID 887—
ProductHCID 12531865HCID 12531865—

Reaction Steps

To a solution of 3.70 g of 5,6,7,8-tetrahydro-1-naphthol, 1.188 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. After cooling to room temperature, the mixture is extracted with 2×75 ml of ether. 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 the product as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04168385
Source datasetuspto-grants-1979_09
ORD IDord-64817e19473a4fea92052e10c8db7fb7
Source noteuspto-grants-1979_09