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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1270735Erstellt: 26. Oktober 2026

Carbon Dioxide → 3-Bromo-6-chloro-2-fluorobenzoic acid

https://huagongshe.com/reaction/1270735

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCarbon DioxideHCID 280—
EduktDiisopropylamineHCID 7912—
Edukt1-Bromo-4-chloro-2-fluorobenzeneHCID 137275—
EduktLithiumHCID 3028194—
EduktButyllithiumHCID 178418339—
LösungsmittelHydrochloric AcidHCID 313—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelAcetone cardiceHCID 18522661—
Produkt3-Bromo-6-chloro-2-fluorobenzoic acidHCID 21742327—

Reaktionsbedingungen

Temperatur-70 °C

Reaktionsschritte

A solution of lithium diiosopropyl amide is generated by adding n-BuLi (360 mL of 2 M solution in THF) to diisopropylamine (73 g, 0.722 mol) in 500 mL of anhydrous THF while a reaction temperature of −60° C. is maintained by cooling in dry-ice acetone bath. After stirring for 30 minutes, 1-bromo-4-chloro-2-fluorobenzene (75 g, 0.36 mol) is added and stirring maintained at −70° C. for 2 hours. The cold solution is then transferred, via a cannula, under an inert atmosphere to a suspension of solid CO2 (100 g, excess) in anhydrous Et2O. The mixture is allowed to warm to room temperature with stirring and then the solvent removed by rotary evaporator. The residual solid is treated with 1 N HCl solution until pH=3.0 and the mixture is filtered. The white solid that is obtained is suspended in 1000 mL of 2 N HCl solution and stirred for an additional 1 hour. The suspension is filtered to collect a white solid which is air dried, suspended in 100 mL of hexanes and collected to give 2-chloro-5-bromo-6-fluorobenzoic acid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07202364B2
Quelldatensatzuspto-grants-2007_04
ORD IDord-6c9ea5fcd81343a7acbd50557642ace7
Quellennotizuspto-grants-2007_04