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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1044702Erstellt: 24. Oktober 2026

Borane → 3-Bromo-5-chlorophenol

https://huagongshe.com/de/reaction/1044702

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 (I), Maleczka, 2003).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08563723B2
Quelldatensatzuspto-grants-2013_10
ORD IDord-2b79712341fa47a1a049f74f73b13afe
Quellennotizuspto-grants-2013_10