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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2273972Erstellt: 26. Oktober 2026

Borane → 3-Bromo-5-chlorophenol

https://huagongshe.com/reaction/2273972

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
PatentnummerUS09126942B2
Quelldatensatzuspto-grants-2015_09
ORD IDord-a5a2626f91834e989eac6b6c555d3aa3
Quellennotizuspto-grants-2015_09