Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1641673Erstellt: 26. Oktober 2026

Ammonium Chloride → (6-Bromo-4-methylpyridin-3-yl)(2,5-difluorophenyl)methanol

https://huagongshe.com/reaction/1641673

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
Edukt2,5-DifluorobenzaldehydeHCID 137663—
Edukt2,5-Dibromo-4-methylpyridineHCID 2734429—
EduktButyllithiumHCID 178418339—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelHexaneHCID 8058—
Produkt(6-Bromo-4-methylpyridin-3-yl)(2,5-difluorophenyl)methanolHCID 5773641434%

Reaktionsschritte

In an argon atmosphere, a hexane solution of n-butyllithium M, 8.22 ml, 13.2 mmol) was added to a solution of 2,5-dibromo-4-methylpyridine (3.00 g, 12.0 mmol) in diethyl ether (120 ml) at −78° C. After stirring the reaction mixture for 30 minutes, 2,5-difluorobenzaldehyde (1.34 ml, 12.0 mmol) was added. After stirring for 1 hour at the same temperature, saturated aqueous ammonium chloride was added at room temperature. After the organic layer was separated, the organic layer was dried over anhydrous sodium sulfate and filtered, and then the filtrate was concentrated under reduced pressure. The resulting residue was subjected to flash silica gel chromatography. The fraction obtained from an elution with hexane:ethyl acetate=4:1 was concentrated under reduced pressure, to obtain the title compound (1.26 g, 4.01 mmol, 34%) as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08114886B2
Quelldatensatzuspto-grants-2012_02
ORD IDord-34104e0a00724cbab9759f5380b05975
Quellennotizuspto-grants-2012_02