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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 4-Phenoxyphenol | HCID 13254 | — |
| Reactant | HCID 22311901 | HCID 22311901 | — |
| Reactant | Potassium tertbutoxide | HCID 50987170 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 4-[(4-Phenoxy)-phenoxy]-butyric acid diethylamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04064269 |
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| Source dataset | uspto-grants-1977_12 |
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| ORD ID | ord-76fb279065bc40a7a878f2a70618ff83 |
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| Source note | uspto-grants-1977_12 |
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