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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 500556Erstellt: 25. Oktober 2026

2-Chloroaniline → 5-Bromo-2-(2-chlorophenylamino)-3,4-difluorobenzoic acid

https://huagongshe.com/reaction/500556

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-ChloroanilineHCID 7240—
EduktDiisopropylamineHCID 7912—
Edukt5-Bromo-2,3,4-trifluorobenzoic acidHCID 11118637—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt5-Bromo-2-(2-chlorophenylamino)-3,4-difluorobenzoic acidHCID 2186699182%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To a solution of i-Pr2NH (25.0 mL, 178 mmol) in THF (200 mL) at 0° C. was added n-BuLi (71.0 mL, 178 mmol, 2.5 M solution in hexanes). After stirring for 15 minutes, this solution was cooled to −78° C. 2-Chloroaniline (12.7 mL, 118 mmol) was added. After vigorous stirring for 10 minutes, a solution of 5-bromo-2,3,4-trifluorobenzoic acid (14.95 g, 58.63 mmol) in THF (30 mL) was added. The dry-ice bath was removed, and the reaction mixture was stirred for 2 hours at room temperature. The mixture was concentrated, treated with 10% aqueous HCl (120 mL), extracted with EtOAc, dried over MgSO4, filtered, and concentrated to give the crude solid which was triturated with boiling CH2Cl2 (125 mL). The yellow solids were filtered, and dried in vacuo to give the desired product (17.4 g, 82%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07772234B2
Quelldatensatzuspto-grants-2010_08
ORD IDord-763cfd38f53343b4988c556c53be055a
Quellennotizuspto-grants-2010_08