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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1754145Erstellt: 27. Oktober 2026

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

https://huagongshe.com/reaction/1754145

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktSodium HydroxideHCID 14798—
EduktMethyl 4-amino-3-chloro-6-(4-cyclopropylphenyl)-5-fluoropicolinateHCID 70497242—
Edukt4-Amino-3-chloro-6-(4-cyclopropylphenyl)-5-fluoropicolinic acidHCID 70497265—
LösungsmittelMethanolHCID 887—
Produkt4-Amino-3-chloro-6-(4-cyclopropylphenyl)-5-fluoropicolinic acidHCID 7049726594%
ProduktBenzyl 4-amino-3-chloro-6-(4-cyclopropylphenyl)-5-fluoropicolinateHCID 70497682—

Reaktionsbedingungen

Temperatur23 °C

Reaktionsschritte

4-Amino-3-chloro-6-(4-cyclopropylphenyl)-5-fluoropicolinic acid. A 2 M solution of aqueous NaOH (600 μL, 1.2 mmol, 2.0 equiv) was added to a stirred suspension of methyl 4-amino-3-chloro-6-(4-cyclopropylphenyl)-5-fluoropicolinate (190 mg, 0.59 mmol, 1.0 equiv) in methyl alcohol (3.0 mL) at 23° C. The resulting heterogeneous white mixture was stirred at 23° C. for 3 h. The reaction mixture was adjusted to approximately pH=4 via dropwise addition of concentrated HCl and then concentrated via rotary evaporation. The residue was slurried in water and vacuum filtered to afford the desired product, 4-amino-3-chloro-6-(4-cyclopropylphenyl)-5-fluoropicolinic acid as a white powder (170 mg, 94% yield): mp 147-149° C.; IR (thin film) 3463 (s), 3339 (s), 3202 (m), 3084 (w), 3007 (w), 1721 (m), 1630 (s) cm−1; 1H NMR (300 MHz, DMSO-d6) δ 7.70 (m, 2H), 7.17 (m, 2H), 6.81 (br s, 2H), 1.96 (m, 1H), 0.99 (m, 2H), 0.71 (m, 2H); ESIMS m/z 307 ([M+H]+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09169217B2
Quelldatensatzuspto-grants-2015_10
ORD IDord-2b5dbb7143a44b13bb6caeca318a52ae
Quellennotizuspto-grants-2015_10