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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2231443Generated: November 3, 2026

Potassium Iodide → [4-Acetyl-3-[3-(4-acetyl-3-hydroxy-2-propylphenoxy)propoxy]-2-propylphenoxy]acetic acid ethyl ester

https://huagongshe.com/reaction/2231443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant2',4'-Dihydroxy-3'-propylacetophenoneHCID 2775198—
Reactant4-Acetyl-3-(3-bromopropoxy)-2-propylphenoxy acetic acid ethyl esterHCID 13389146—
SolventAcetoneHCID 180—
SolventDimethylformamideHCID 6228—
Product[4-Acetyl-3-[3-(4-acetyl-3-hydroxy-2-propylphenoxy)propoxy]-2-propylphenoxy]acetic acid ethyl esterHCID 1338914868%

Reaction Steps

A mixture of 1.17 g of 1-(2,4-dihydroxy-3-propylphenyl)ethanone, 2.41 g of 4-acetyl-3-(3-bromopropoxy)-2-propylphenoxy acetic acid ethyl ester, 1.66 g of anhydrous potassium carbonate and 0.1 g of potassium iodide in 15 ml of anhydrous acetone and 15 ml of anhydrous dimethylformamide was stirred at reflux for 18 hours. The solvent was removed in vacuo, 50 ml of 0.1N hydrochloric acid was added to the residue and the product was extracted with methylene chloride. The dried, over sodium sulfate, extract was concentrated in vacuo and the crude product was crystallized from methanol to yield 2.1 g, mp 45°-46°, (68% yield) of [4-acetyl-3-[3-(4-acetyl-3-hydroxy-2-propylphenoxy)propoxy]-2-propylphenoxy]acetic acid ethyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04782176
Source datasetuspto-grants-1988_11
ORD IDord-3a3d9d363e2f4390b0a9fe057c52c046
Source noteuspto-grants-1988_11