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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 461877Generated: October 29, 2026

Diethyl Ether → 4-[(4-Phenoxy)-phenoxy]-butyric acid diethylamide

https://huagongshe.com/reaction/461877

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
Reactant4-PhenoxyphenolHCID 13254—
ReactantHCID 22311901HCID 22311901—
ReactantPotassium tertbutoxideHCID 50987170—
SolventDimethyl SulfoxideHCID 679—
Product4-[(4-Phenoxy)-phenoxy]-butyric acid diethylamideHCID 54272619—

Reaction Steps

17 g of potassium-tert.-butanolate is added at 10° C to a solution of 28 g of 4-phenoxy-phenol in 100 ml of anhydrous dimethylsulphoxide. After the base has completely dissolved, an addition is made dropwise in the course of 2 hours, with stirring, of 26.5 g of chlorobutyric acid diethylamide dissolved in 20 ml of dimethylsulphoxide and the whole is further stirred overnight at room temperature. For further processing, the reaction mixture is poured into ice water, and extraction is repeatedly performed with diethyl ether. The combined ether phases are washed four times with cold 10% potassium hydroxide solution and subsequently repeatedly with water; they are then dried by means of sodium sulphate. After the ether has been distilled off, there is obtained crude 4-[(4-phenoxy)-phenoxy]-butyric acid diethylamide, which is purified by chromatography on silica gel (eluant: ether/hexane 1:3), and recrystallised from isopropanol/hexane, M.P. 73°-74° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04064269
Source datasetuspto-grants-1977_12
ORD IDord-76fb279065bc40a7a878f2a70618ff83
Source noteuspto-grants-1977_12