HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 406454Generated: October 26, 2026
Halauxifen-methyl → Methyl 4-(acetylamino)-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)pyridine-2-carboxylate
https://huagongshe.com/reaction/406454
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Halauxifen-methyl | HCID 16656802 | — |
| Reactant | 4-Chloro-2-fluoro-3-methoxyphenylboronic acid | HCID 44129706 | — |
| Solvent | Methyl Isobutyl Ketone | HCID 7909 | — |
| Product | Methyl 4-(acetylamino)-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)pyridine-2-carboxylate | HCID 67210962 | — |
Reaction Steps
An embodiment of the present disclosure includes a method of producing methyl 4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)pyridine-2-carboxylate. The method comprises adding methyl isobutyl ketone to an aqueous solution comprising 4-chloro-2-fluoro-3-methoxyphenylboronic acid to form an organic phase comprising the 4-chloro-2-fluoro-3-methoxyphenylboronic acid and an aqueous phase. The organic phase and the aqueous phase are separated. The 4-chloro-2-fluoro-3-methoxyphenylboronic acid is reacted with methyl 4-(acetylamino)-3,6-dichloropyridine-2-carboxylate in methyl isobutyl ketone to produce methyl 4-(acetylamino)-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)pyridine-2-carboxylate, which is deacetylated to produce methyl 4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)pyridine-2-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08754110B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-faef2dc7331b4291ad9f60f89e3d5d8d |
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| Source note | uspto-grants-2014_06 |
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