HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1774283Generated: October 31, 2026
Water → Methyl 4-(4-methoxyphenylamino)-5-fluoro-6-(4-chlorophenyl)picolinate
https://huagongshe.com/reaction/1774283
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 4-Chlorobenzylamine | HCID 66036 | — |
| Reactant | Methyl 5,5,5-trifluoro-4-((4-methoxyphenyl)imino)pent-2-ynoate | HCID 86723348 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 4-(4-methoxyphenylamino)-5-fluoro-6-(4-chlorophenyl)picolinate | HCID 86723349 | — |
Reaction Steps
In a typical reaction, methyl 5,5,5-trifluoro-4-((4-methoxyphenyl)imino)pent-2-ynoate is mixed with about a 2.5 to 3 fold excess of 4-chlorobenzyl amine and about a 2.5 to 3 fold excess of cesium carbonate in anhydrous terahydrofuran. The mixture is heated at about 80° C. until the reaction is complete. After cooling, an extraction solvent like a halogenated hydrocarbon is added to the mixture along with water. The organic layer is recovered, washed with brine and dried. The solvent is evaporated to provide crude methyl 4-(4-methoxyphenylamino)-5-fluoro-6-(4-chlorophenyl)picolinate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09260392B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-42ca26dd47d4421bb29c66756e311409 |
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| Source note | uspto-grants-2016_02 |
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