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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 577285Erstellt: 24. Oktober 2026

Carbon Dioxide → 3-Bromo-2,5,6-trifluorobenzoic acid

https://huagongshe.com/de/reaction/577285

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCarbon DioxideHCID 280—
EduktHydrochloric AcidHCID 313—
EduktDiisopropylamineHCID 7912—
Edukt1-Bromo-2,4,5-trifluorobenzeneHCID 67597—
EduktLithium diisopropylamideHCID 2724682—
EduktButyllithiumHCID 178418339—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-Bromo-2,5,6-trifluorobenzoic acidHCID 1427882552,3%

Reaktionsschritte

n-Butyllithium (2.5M in hexane, 10.5 mL, 1.1 eq.) was added dropwise over 15 min to a solution of diisopropylamine (4.0 mL, 1.2 eq.) in THF (25 mL) at 0° C. After stirring for 15 min, the LDA solution was added dropwise over 40 min to a solution of 2,4,5-trifluorobromobenzene (5.0 g, 24 mmol) in THF (50 mL) at −78° C. The solution was stirred for 10 min and then transferred to a slurry of dry ice (50 g) in diethylether (65 mL). The reaction was allowed to warm to rt and treated with 1M HCl. The phases were separated and the organic layer extracted with 0.5M NaOH. The basic extracts were acidified to pH 1 with 6M HCl and extracted with diethylether. The combined organic phases were dried over sodium sulfate and evaporated to yield 3-bromo-2,5,6-trifluorobenzoic acid as a white solid (3.2 g, 52%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09040545B2
Quelldatensatzuspto-grants-2015_05
ORD IDord-8b1b2365dc3c4641836a9106b2ab1788
Quellennotizuspto-grants-2015_05