HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649300Generated: November 1, 2026
Dimethylformamide → Ethyl 4-[3,5-bis(trifluoromethyl)phenoxy]butanoate
https://huagongshe.com/reaction/1649300
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 3,5-Bis(trifluoromethyl)phenol | HCID 67680 | — |
| Reactant | Ethyl 4-bromobutyrate | HCID 76300 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Ethyl 4-[3,5-bis(trifluoromethyl)phenoxy]butanoate | HCID 13242433 | 95% |
Reaction Steps
To a stirred solution containing 11.5 g (0.05 mole) of 3,5-ditrifluoromethylphenol, 3.3 g (0.05 mole) of 85% potassium hydroxide, 200 ml of N,N-dimethylformamide and 10 ml of water, 0.055 mole of ethyl 4-bromobutyrate was added in one portion. The stirred reaction mixture was heated at 80°-90° C. for 24 hours. After cooling to 25° C., 500 ml of water and 500 ml of ethyl ether were added; and stirring was continued for 15 minutes. The separated ether layer was washed with water until neutral to litmus and dried over sodium sulfate. The ether was removed in vacuo at a maximum temperature of 80°-90° C. at 1-2 mm of Hg. A product with a ND25 =1.4281 was obtained with a 95% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04416687 |
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| Source dataset | uspto-grants-1983_11 |
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| ORD ID | ord-90a43baef6d74f50b2b601f1ea7df2e6 |
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| Source note | uspto-grants-1983_11 |
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