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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-Methyl-2-buteneHCID 10553—
ReactantSodium Phosphate, DibasicHCID 24203—
ReactantSodium ChloriteHCID 23668197—
ReactantHCID 86723380HCID 86723380—
Solvent2-Methylpropan-2-ol--water (1/1)HCID 71401949—
Product4-Amino-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoropyridine-2-carboxylic acidHCID 86723381—

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096526B2
Source datasetuspto-grants-2015_08
ORD IDord-06049c7b863b4c1f9ebd33cb986f1699
Source noteuspto-grants-2015_08