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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1094800Erstellt: 26. Oktober 2026

Ethylenediaminetetraacetic Acid → (5-Chloro-2-(trifluoromethoxy)phenyl)boronic acid

https://huagongshe.com/reaction/1094800

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthylenediaminetetraacetic AcidHCID 6049—
EduktCyclohexaneHCID 8078—
Edukt1-Chloro-4-(trifluoromethoxy)benzeneHCID 2777273—
EduktFluorodimethoxyboraneHCID 3083563—
EduktCID 53628100HCID 178418400—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(5-Chloro-2-(trifluoromethoxy)phenyl)boronic acidHCID 53216719—

Reaktionsschritte

To a solution of the 4-chloro(trifluoromethoxy)benzene (2.0 g, 10.18 mmol) in dry tetrahydrofuran (THF, 30 ml) at −78° C., was added ethylenediaminetetraacetic acid (EDTA, 1.24 g, 10.7 mmol) followed by a 1.3 M solution of sec-butyllithium in cyclohexane (7.63 ml, 10.7 mmol) and the reaction stirred for 2 hours under nitrogen. To this reaction mixture at −78° C., was then added dropwise the preformed dimethoxyfluoroborane mixture. The reaction was stirred at −78° C. for 30 minutes, warmed to room temperature for 30 minutes, and then quenched with water (10 ml). The reaction mixture was extracted with diethyl ether (4×50 ml). The combined organic extracts were dried over MgSO4 and concentrated in vacuo. To purify, the residue was dissolved in diethyl ether (10 ml) and washed with an aqueous solution of 10% NaOH (50 ml). The aqueous layer was acidified and extracted with ethyl acetate (3×40 ml). The combined ethyl acetate extracts were dried over MgSO4 and concentrated in vacuo to afford a mixture of the title compound and its corresponding regioisomer as a white solid (0.862 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08134007B2
Quelldatensatzuspto-grants-2012_03
ORD IDord-0d1e6e05ceb246bfac11c2f48e955d55
Quellennotizuspto-grants-2012_03