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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 871978Erstellt: 25. Oktober 2026

Hydrochloric Acid → (5-Chloro-4-fluoro-2-methoxyphenyl)boronic acid

https://huagongshe.com/reaction/871978

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktIsopropyldiisopropoxyboraneHCID 13583183—
Edukt1-Bromo-5-chloro-4-fluoro-2-methoxybenzeneHCID 53217087—
EduktButyllithiumHCID 178418339—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelHexaneHCID 8058—
LösungsmittelEthyl AcetateHCID 8857—
Produkt(5-Chloro-4-fluoro-2-methoxyphenyl)boronic acidHCID 5767187689%

Reaktionsbedingungen

Temperatur-40 °C

Reaktionsschritte

2-Bromo-4-chloro-5-fluoroanisole (Reference Compound No. 16-1, 239 mg, 1.00 mmol) was dissolved in mixed solvent of anhydrous toluene (2 mL) and anhydrous tetrahydrofuran (0.5 mL), 1.6M hexane solution of n-butyl lithium (750 μL, 1.20 mmol) was added thereto at −40° C., and then the reaction mixture was stirred at the same temperature for 30 minutes. Triisopropyl boronic acid (277 μL, 1.20 mmol) was added dropwise to the reaction mixture, warmed to −20° C. over 10 minutes, and then 2N aqueous HCl solution (1 mL) was added. After the reaction mixture was stirred at room temperature for 20 minutes, ethyl acetate (20 mL) and water (20 mL) were added and partitioned. The organic layer was washed with saturated brine (20 mL), dried over anhydrous magnesium sulfate, and then the solvent was removed under reduced pressure to give the titled reference compound (181 mg) as a colorless solid. (Yield 89%)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08975256B2
Quelldatensatzuspto-grants-2015_03
ORD IDord-a44cfd994e4d492ba66244a24bbfa100
Quellennotizuspto-grants-2015_03