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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1704046Generated: October 27, 2026

Potassium Iodide → Methyl alpha-(p-cyclohexylphenoxy)-alpha-[p-(p-chlorophenoxy)phenyl]acetate

https://huagongshe.com/reaction/1704046

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant4-CyclohexylphenolHCID 14327—
ReactantSodium MethoxideHCID 10942334—
ReactantMethyl alpha-Bromo-alpha-[p-(p-chlorophenoxy)phenyl]acetateHCID 20392594—
SolventBenzeneHCID 241—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductMethyl alpha-(p-cyclohexylphenoxy)-alpha-[p-(p-chlorophenoxy)phenyl]acetateHCID 20392628—

Reaction Steps

To a solution of 1.19 g of sodium methoxide and 4.4 g of p-cyclohexylphenol in 40 ml of methanol is added 50 mg of potassium iodide and 7.11 g of methyl α-bromo-α-[p-(p-chlorophenoxy)phenyl]acetate in 10 ml of benzene. The solution is refluxed overnight, cooled to room temperature and poured into 100 ml of water. The mixture is extracted with two 60 ml portions of ether and the combined extracts washed with two 50 ml portins of 5% sodium hydroxide, 50 ml of water and 50 ml of saturated NaCl. The extract is dried (MgSO4) and the solvent removed under vacuum. The residue is triturated with petroleum ether to give the product as white crystals, mp 122°-123.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04125729
Source datasetuspto-grants-1978_11
ORD IDord-63c4c26669294580b7226adc96b4af16
Source noteuspto-grants-1978_11