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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164942Generated: October 25, 2026

Potassium Carbonate → 4-[4-Acetyl-3-[2-[2-[(methylsulfonyl)oxy]ethoxy]-ethoxy]-2-propylphenoxy]butanoic acid ethyl ester

https://huagongshe.com/reaction/2164942

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantDiethylene Glycol DimethanesulfonateHCID 147571—
ReactantEthyl 4-(4-acetyl-3-hydroxy-2-propylphenoxy)butanoateHCID 14330004—
SolventAcetoneHCID 180—
SolventDimethylformamideHCID 6228—
Product4-[4-Acetyl-3-[2-[2-[(methylsulfonyl)oxy]ethoxy]-ethoxy]-2-propylphenoxy]butanoic acid ethyl esterHCID 1433000967%

Reaction Steps

A mixture of 4 g (0.013 mol) of 4-(4-acetyl-3-hydroxy-2-propylphenoxy)butanoic acid ethyl ester, 17 g (0.065 mol) of diethylene glycol dimesylate and 3.6 g (0.026 mol) of anhydrous potassium carbonate in 80 ml of anhydrous acetone and 40 ml of anhydrous dimethylformamide was stirred at reflux for 20 hours. An additional 1.8 g of potassium carbonate was added and reflux was continued for a total of 44 hours. The reaction mixture was filtered and concentrated in vacuo to an orange oil which was treated with ethyl acetate and sodium chloride solution. The yellow oil obtained on concentration of the ethyl acetate was purified by HPLC, eluting with 15% ethyl acetate/toluene to yield 4.1 g (67% yield) of 4-[4-acetyl-3-[2-[2-[(methylsulfonyl)oxy]ethoxy]-ethoxy]-2-propylphenoxy]butanoic acid ethyl ester as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04507498
Source datasetuspto-grants-1985_03
ORD IDord-89540108dfe34b4899e1f52f14e30356
Source noteuspto-grants-1985_03