HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1589717Generated: November 4, 2026
Diethylamine → N,N-diethyl-2-[4-(5-trifluoromethyl-2-pyridyloxy)phenoxy]propionic acid amide
https://huagongshe.com/reaction/1589717
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(4-{[5-(Trifluoromethyl)pyridin-2-yl]oxy}phenoxy)propanoyl chloride | HCID 13055220 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | N,N-diethyl-2-[4-(5-trifluoromethyl-2-pyridyloxy)phenoxy]propionic acid amide | HCID 54279405 | — |
Reaction Steps
3.4 g (0.046 mol) of diethylamine and 4.8 g (0.47 mol) of triethylamine dissolved in 10 ml of benzene are dropped into the solution of 15.6 g (0.045 mol) of 2-[4-(5-trifluoromethyl-2-pyridyloxy)phenoxy]propionyl chloride in 40 ml of anhydrous benzene at 0°-5° C. under stirring. After termination of the portionwise addition, the reaction mixture is stirred for additional 2 hours whilst it is allowed to warm to room temperature. The mixture is filtered off, the precipitate is washed with a little volume of ether, the filtrate is washed first with 5% hydrochloric acid and then with saturated sodium chloride solution, then dried over anhydrous magnesium sulfate and finally evaporated to dryness. The crude product is purified by chromatography on a column filled with silica gel of 0.063-0.2 mm particle size by using a 4:1 mixture of n-hexane/acetone for elution.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05199970 |
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| Source dataset | uspto-grants-1993_04 |
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| ORD ID | ord-ff56c5794e16498c8cf7e47adfa61959 |
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| Source note | uspto-grants-1993_04 |
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