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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655640Generated: October 30, 2026

Acetone → 2-(4-Acetamidophenoxy)-2-methylpropanoic acid

https://huagongshe.com/reaction/1655640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantAcetaminophenHCID 1983—
ReactantChloroformHCID 6212—
ReactantSodium HydroxideHCID 14798—
Reactant2-(4-Aminophenoxy)-2-methylpropanoic acidHCID 2774958—
Product2-(4-Acetamidophenoxy)-2-methylpropanoic acidHCID 1487985560%

Reaction Steps

FIG. 2A illustrates a reaction scheme for preparing 2-(4-aminophenoxy)-2-methyl propionic acid, a compound that is useful as a precursor in the preparation of Group I compounds. In accordance with the scheme of FIG. 2A, 8 grams (g) (0.2 mol) of pulverized sodium hydroxide is added to a suspension of 5.28 g (0.035 mol) of p-acetaminophenol in 23 g (0.4 mol) of acetone. The reaction mixture is stirred at room temperature for 1/2 hour. Subsequently, 3.58 g (0.03 mol) of chloroform is added dropwise over the course of 30 minutes. The reaction mixture is stirred overnight at room temperature and acetone is removed under vacuum. The residue is dissolved in water (10 ml), followed by acidification with 37% hydrochloric acid (HCl) to produce a pale yellow precipitate of 2-(4-acetaminophenoxy)-2-methyl propionic acid (5 g, 60% yield), crystallized from methanol, mp 69°-71° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05250701
Source datasetuspto-grants-1993_10
ORD IDord-81102b19e1e84ab7b289379641bdebfe
Source noteuspto-grants-1993_10