Hydrochloric Acid → 4-Fluoro-2-formylphenylboronic Acid (contains varying amounts of Anhydride)

HRID 1951694

Reaktionsgleichung

Reaktionsgleichung von HRID 1951694
Br[C:2]1[CH:7]=[CH:6][C:5]([F:8])=[CH:4][C:3]=1[CH:9]1[O:13]CCO1.C([Li])CCC.[B:19](OC(C)C)([O:24]C(C)C)[O:20]C(C)C.Cl>O1CCCC1.CCCCCC.O>[F:8][C:5]1[CH:6]=[CH:7][C:2]([B:19]([OH:24])[OH:20])=[C:3]([CH:9]=[O:13])[CH:4]=1

Komponenten

8

Reaktionsbedingungen

Temperatur
-74 °C

Versuchsvorschrift

To a solution of 2.30 g (9.31 mmol) 2-(2-bromo-5-fluoro-phenyl)-[1,3]dioxolane in 15 ml tetrahydrofuran was added dropwise at −70° C. 6.11 ml (9.77 mmol) of a 1.6 M solution of n-butyllithium in hexane. The reaction mixture was stirred at −74° C. for 1 h. After dropwise addition of 2.65 ml (11.2 mmol) triisopropyl borate at −70° C. the reaction mixture was allowed to warm to 15° C. during a period of 2 h. Water (7 ml) was added, and the mixture was acidified to pH 1 by addition of 37% hydrochloric acid solution. After heating at 60° C. for 1 h, the mixture was cooled to room temperature and extracted with three 50-ml portions of diethyl ether. The combined organic layers were washed with 50 ml brine, dried over sodium sulfate and concentrated. Flash chromatography gave 1.2 g (77%) of the title compound as a light yellow liquid.

Aufarbeitung

  1. temperatureto warm to 15° C. during a period of 2 h
  2. temperatureAfter heating at 60° C. for 1 h
  3. temperaturethe mixture was cooled to room temperature
  4. extractionextracted with three 50-ml portions of diethyl ether
  5. washThe combined organic layers were washed with 50 ml brine
  6. dry with materialdried over sodium sulfate
  7. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-2db20d8a20dd41c391dd10652bd703b2
Quelldatensatz
uspto-grants-2013_03
Patentnummer
US08404708B2

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