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HRID 1044702作成日:2026年10月26日

Borane → 3-Bromo-5-chlorophenol

https://huagongshe.com/reaction/1044702

反応式

関与物質

役割名称HCID仕込み量
反応物BoraneHCID 6331—
反応物1-Bromo-3-chlorobenzeneHCID 7928—
反応物1,2-Bis(dimethylphosphino)ethaneHCID 141059—
反応物PinacolboraneHCID 6364989—
反応物Potassium hydroxy sulfiteHCID 23707502—
触媒(1,5-cyclooctadiene)-eta5-indenyl)iridium(I)HCID 178420247—
溶媒AcetoneHCID 180—
溶媒WaterHCID 962—
生成物3-Bromo-5-chlorophenolHCID 2263018062%

反応条件

温度150 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08563723B2
出典データセットuspto-grants-2013_10
ORD IDord-2b79712341fa47a1a049f74f73b13afe
出典メモuspto-grants-2013_10