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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1863324Generated: November 1, 2026

Potassium Iodide → HCID 12531863, compound

https://huagongshe.com/reaction/1863324

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant1-NaphtholHCID 7005—
ReactantSodium MethoxideHCID 10942334—
ReactantMethyl alpha-Bromo-alpha-[p-(p-chlorophenoxy)phenyl]acetateHCID 20392594—
SolventBenzeneHCID 241—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 12531863HCID 12531863—

Reaction Steps

To a solution of 3.60 g of 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 solution is refluxed overnight and then poured into 100 ml of water. The mixture is extracted with 2×75 ml of ether. The combined extracts are washed with 2×50 ml of 5% NaOH, 50 ml of water, saturated brine and dried (MgSO4). Evaporation of the solvent yields a red oil. Chromatography on 100 g of silica gel (benzene, 400 ml) affords a pink oil which solidifies on trituration with petroleum ether to yield a pink solid, mp 107°-109.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04168385
Source datasetuspto-grants-1979_09
ORD IDord-f525b103a1174aaa9cd500b1ef1b72c0
Source noteuspto-grants-1979_09