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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1704022Generated: October 30, 2026

4-Chlorophenol → Methyl(p-chlorophenoxy)[p-(p-chlorophenoxy)phenyl]acetate

https://huagongshe.com/reaction/1704022

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChlorophenolHCID 4684—
ReactantPotassium IodideHCID 4875—
ReactantSodium MethoxideHCID 10942334—
ReactantMethyl alpha-Bromo-alpha-[p-(p-chlorophenoxy)phenyl]acetateHCID 20392594—
SolventBenzeneHCID 241—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductMethyl(p-chlorophenoxy)[p-(p-chlorophenoxy)phenyl]acetateHCID 12531843—

Reaction Steps

To a solution of 1.19 g of sodium methoxide in 40 ml of methanol is added 3.21 g of 4-chlorophenol. A few crystals of potassium iodide are added, followed by a solution of 7.11 g of methyl α-bromo-α-[p-(p-chlorophenoxy)phenyl]acetate in 10 ml of benzene. The solution is heated at reflux overnight. After cooling to room temperature, the solution is poured into 100 ml of water and extracted with two 100 ml portions of ether. The combined extracts are washed with 50 ml of 5% NaOH, 50 ml of saturated brine and dried over MgSO4. The solvent is evaporated at reduced pressure and the residue is triturated with petroleum ether to give the product as white crystals, mp 100°-101.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04125729
Source datasetuspto-grants-1978_11
ORD IDord-ce291fabee4e4c4f837476db12152eb8
Source noteuspto-grants-1978_11