HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 508541Generated: November 1, 2026
Hydrochloric Acid → 4-Amino-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoropyridine-2-carboxylic acid
https://huagongshe.com/reaction/508541
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-Methyl-2-butene | HCID 10553 | — |
| Reactant | Sodium Phosphate, Dibasic | HCID 24203 | — |
| Reactant | Sodium Chlorite | HCID 23668197 | — |
| Reactant | HCID 86723380 | HCID 86723380 | — |
| Solvent | 2-Methylpropan-2-ol--water (1/1) | HCID 71401949 | — |
| Product | 4-Amino-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoropyridine-2-carboxylic acid | HCID 86723381 | — |
Reaction Steps
In a typical reaction, 4-amino-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoropicolinaldehyde is oxidized with an excess of sodium chlorite, between 20-30 equivalents of 2-methyl-2-butene and about 5 equivalents of disodium hydrogen phosphate in a t-butanol/water mixture. The mixture is heated at about 80° C. until the reaction is complete. After cooling, the mixture is treated with dilute hydrochloric acid and extracted with ethyl acetate. The organic layer is separated and dried. The solvent is evaporated to provide crude 4-amino-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoropicolinic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09096526B2 |
|---|
| Source dataset | uspto-grants-2015_08 |
|---|
| ORD ID | ord-06049c7b863b4c1f9ebd33cb986f1699 |
|---|
| Source note | uspto-grants-2015_08 |
|---|