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
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 | 4-Amino-3-chloro-6-(4-chlorophenyl)-5-fluoropicolinaldehyde | HCID 86723353 | — |
| Solvent | 2-Methylpropan-2-ol--water (1/1) | HCID 71401949 | — |
| Product | 4-Amino-3-chloro-6-(4-chlorophenyl)-5-fluoropicolinic acid | HCID 22677324 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09212141B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-aecced2643774214b57effedb7404075 |
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| Source note | uspto-grants-2015_12 |
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