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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1863303Generated: November 1, 2026

3,4,5-Trichlorophenol → HCID 12531851, compound

https://huagongshe.com/reaction/1863303

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4,5-TrichlorophenolHCID 11859—
ReactantSodium MethoxideHCID 10942334—
ReactantMethyl alpha-Bromo-alpha-[p-(p-chlorophenoxy)phenyl]acetateHCID 20392594—
SolventBenzeneHCID 241—
SolventMethanolHCID 887—
SolventPotassium IodideHCID 4875—
SolventChloroformHCID 6212—
ProductHCID 12531851HCID 12531851—

Reaction Steps

To a solution of 4.93 g of 3,4,5-trichlorophenol and 1.19 g of sodium methoxide 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 and 50 mg of potassium iodide. The mixture is refluxed for 20 hours and the solvent removed in vacuo. To the residue is added water and the mixture is extracted with ether. The ether extracts are washed with 10% potassium carbonate and with water and dried (MgSO4). Evaporation of the solvent under vacuum gives a tan oil. The oil is dissolved in chloroform and filtered through a column of silica gel. Removal of the solvent from the second 200 ml cut gives the product as a tan oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04168385
Source datasetuspto-grants-1979_09
ORD IDord-61a057739ad14201a40aa486ccf675ea
Source noteuspto-grants-1979_09