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HRID 1641697Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1641697

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
Edukt2,3,6-TrifluorobenzaldehydeHCID 517845—
Edukt2,5-Dibromo-4-methylpyridineHCID 2734429—
EduktButyllithiumHCID 178418339—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelHexaneHCID 8058—
Produkt(6-Bromo-4-methylpyridin-3-yl)(2,3,6-trifluorophenyl)methanolHCID 8663115081,8%

Reaktionsschritte

A hexane solution of n-butyllithium (1.54 M, 12.2 ml, 18.7 mmol) was added to a solution of 2,5-dibromo-4-methylpyridine (4.27 g, 17.0 mmol) in diethyl ether (200 ml) in an argon atmosphere at −78° C. After stirring the reaction mixture for 30 minutes, 2,3,6-trifluorobenzaldehyde (1.99 ml, 17.0 mmol) was added thereto. After stirring for 30 minutes at the same temperature, saturated aqueous ammonium chloride was added to the mixture at room temperature. The organic layer was dried over anhydrous sodium sulfate and filtered, then the filtrate was concentrated under reduced pressure, and 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 (4.60 g, 13.9 mmol, 81%) as a pale yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08114886B2
Quelldatensatzuspto-grants-2012_02
ORD IDord-e9ca1cc13c424495b5ada26415834050
Quellennotizuspto-grants-2012_02