HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1589715Generated: November 4, 2026
Allylamine → N-allyl-2-[4-(5-trifluoromethyl-2-pyridyloxy)phenoxy]-propionic acid amide
https://huagongshe.com/reaction/1589715
Participants
| Role | Name | HCID | Charge |
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| Reactant | Allylamine | HCID 7853 | — |
| Reactant | Fluazifop-methyl | HCID 155294 | — |
| Product | N-allyl-2-[4-(5-trifluoromethyl-2-pyridyloxy)phenoxy]-propionic acid amide | HCID 53760130 | — |
Reaction Steps
A mixture containing 11.85 g (0.035 mol) of methyl 2-[4-(5-trifluoromethyl-2-pyridyloxy)phenoxy]-propionate and 11.5 g (0.2 mol) of allylamine is boiled under reflux (about 60° C.) for 10 hours. (The reaction is followed by gas chromatography.) Thereafter, the excess of allylamine is distilled off and the residue is dissolved in benzene. After washing the solution cooled down with 5% aqueous hydrochloric acid and then with saturated sodium chloride solution, the organic phase is dried over anhydrous magnesium sulfate and evaporated. The crude product is recrystallized from petroleum ether (b.p. 120° C.) containing a small amount of toluene.
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-0b5d0fcbd1944a6bbe83be6dfbb0c587 |
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| Source note | uspto-grants-1993_04 |
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