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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1704111Generated: November 1, 2026

Benzene → Methyl(m-tert.-butylphenoxy){p-[3-(p-chlorophenoxy)propoxy]phenyl}acetate

https://huagongshe.com/reaction/1704111

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantPhenol, 3-(1,1-dimethylethyl)-HCID 11450—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 22761172HCID 22761172—
CatalystPotassium IodideHCID 4875—
SolventMethanolHCID 887—
ProductMethyl(m-tert.-butylphenoxy){p-[3-(p-chlorophenoxy)propoxy]phenyl}acetateHCID 13171133748.9%

Reaction Steps

To a mixture of 8.27 g of methyl bromo{p-[3-(p-chlorophenoxy)propoxy]phenyl}acetate, 3.75 g of m-tert.-butylphenol, 10 ml of benzene and 40 ml of methanol is added 1.19 g of sodium methoxide and 50 mg of potassium iodide. The mixture is refluxed for 24 hours and the solvent removed under reduced pressure. To the residue is added acetone and hexane and the mixture is filtered. The filtrate is dried (MgSO4) and concentrated under reduced pressure to give an oil. The oil is chromatographed over silica gel with dichloromethane as eluent to give 4.72 g of product as a colorless viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04125732
Source datasetuspto-grants-1978_11
ORD IDord-a0a3d0f33cc244d783f3d92614b3d5c4
Source noteuspto-grants-1978_11