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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503104Generated: October 30, 2026

Hydrochloric Acid → 4-Amino-3-chloro-6-(4-chlorophenyl)-5-fluoropicolinic acid

https://huagongshe.com/reaction/1503104

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-Methyl-2-buteneHCID 10553—
ReactantSodium Phosphate, DibasicHCID 24203—
ReactantSodium ChloriteHCID 23668197—
Reactant4-Amino-3-chloro-6-(4-chlorophenyl)-5-fluoropicolinaldehydeHCID 86723353—
Solvent2-Methylpropan-2-ol--water (1/1)HCID 71401949—
Product4-Amino-3-chloro-6-(4-chlorophenyl)-5-fluoropicolinic acidHCID 22677324—

Reaction Conditions

Temperature80 °C

Reaction Steps

In a typical reaction, 4-amino-3-chloro-6-(4-chlorophenyl)-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-butyl alcohol/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-3-chloro-6-(4-chlorophenyl)-5-fluoropicolinic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212141B2
Source datasetuspto-grants-2015_12
ORD IDord-aecced2643774214b57effedb7404075
Source noteuspto-grants-2015_12