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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1704040Generated: October 30, 2026

Acetaminophen → Methyl alpha-(p-acetamidophenoxy)-alpha-[p-(p-chlorophenoxy)phenyl]acetate

https://huagongshe.com/reaction/1704040

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaminophenHCID 1983—
ReactantPotassium IodideHCID 4875—
ReactantSodium MethoxideHCID 10942334—
ReactantMethyl alpha-Bromo-alpha-[p-(p-chlorophenoxy)phenyl]acetateHCID 20392594—
SolventBenzeneHCID 241—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductMethyl alpha-(p-acetamidophenoxy)-alpha-[p-(p-chlorophenoxy)phenyl]acetateHCID 12531907—

Reaction Steps

To a solution of 3.78 g of p-acetamidophenol, 1.1 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 15 ml of benzene. The mixture is refluxed for 20 hours, poured into ice and water and extracted with chloroform. The chloroform extracts are washed with 10% potassium carbonate and with water. The extract is dried over magnesium sulfate and concentrated to a gum under vacuum. Petroleum ether is added to the residue and several ml of acetone. Scratching the flask gives crystals which are filtered to give the product as pink crystals, mp 152°- 157° C. The crystals are dissolved in a minimum amount of hot acetone, the solution chilled and diluted with petroleum ether. Chilling and filtering gives pale pink crystals, mp 157°-160° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04125729
Source datasetuspto-grants-1978_11
ORD IDord-477bc9b6df5348bdb5f6dcc97324db4a
Source noteuspto-grants-1978_11