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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1396057Erstellt: 27. Oktober 2026

Borane → 3-Bromo-5-chlorophenol

https://huagongshe.com/reaction/1396057

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBoraneHCID 6331—
Edukt1-Bromo-3-chlorobenzeneHCID 7928—
Edukt1,2-Bis(dimethylphosphino)ethaneHCID 141059—
EduktPinacolboraneHCID 6364989—
EduktPotassium hydroxy sulfiteHCID 23707502—
Katalysator(1,5-cyclooctadiene)-eta5-indenyl)iridium(I)HCID 178420247—
LösungsmittelAcetoneHCID 180—
LösungsmittelWaterHCID 962—
Produkt3-Bromo-5-chlorophenolHCID 2263018062%

Reaktionsbedingungen

Temperatur150 °C

Reaktionsschritte

Under an atmosphere of dry nitrogen, 103 mg 1,5-cyclooctadiene(H5-indenyl)iridium (I) was put in a 25 mL Pyrex bottle. Subsequently were added 0.04 mL 1,2-bis(dimethylphosphino)ethane, 0.61 mL 3-bromochlorobenzene and 1.52 mL pinacolborane. The mixture was stirred at 150° C. for 3.5 h. After cooling to room temperature, the borane adduct was taken up in 17 mL acetone to give a clear solution. This solution was added slowly to 17.41 mL of a 0.30 M solution of oxone in water cooled in an ice bath. The mixture was stirred vigorously for 15 min. at room temperature and extracted three times with DCM. The combined organic phases were dried over Na2SO4 and evaporated to dryness. The residue was purified by flash chromatography (DCM) to yield 750 mg (62%) of a beige solid. 1H NMR complies with known data (compound (1), Maleczka, 2003).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08901108B2
Quelldatensatzuspto-grants-2014_12
ORD IDord-97150a3b1f58414499f4b9460bae2055
Quellennotizuspto-grants-2014_12