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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1863319Generated: October 26, 2026

Potassium Iodide → Methyl alpha-(3,5-di-tert-butylphenoxy)-alpha-[p-(p-chlorophenoxy)phenyl]acetate

https://huagongshe.com/reaction/1863319

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant3,5-Di-tert-butylphenolHCID 70825—
ReactantSodium MethoxideHCID 10942334—
ReactantMethyl alpha-Bromo-alpha-[p-(p-chlorophenoxy)phenyl]acetateHCID 20392594—
SolventBenzeneHCID 241—
SolventMethanolHCID 887—
ProductMethyl alpha-(3,5-di-tert-butylphenoxy)-alpha-[p-(p-chlorophenoxy)phenyl]acetateHCID 12531858—

Reaction Steps

To a solution of 5.16 g of 3,5-di-tert-butylphenol 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 heated at reflux overnight and worked up as described in Example 70 to yield a yellos oil which is purified by chromatography on 100 of silica gel (benzene, 400 ml) and pumped in vacuo at 120° C. (0.05 mm) to yield a yellow glass.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04168385
Source datasetuspto-grants-1979_09
ORD IDord-ab4db61f2a494946b017ff014304c1fd
Source noteuspto-grants-1979_09