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HRID 1641673作成日:2026年10月27日

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

https://huagongshe.com/reaction/1641673

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物2,5-DifluorobenzaldehydeHCID 137663—
反応物2,5-Dibromo-4-methylpyridineHCID 2734429—
反応物ButyllithiumHCID 178418339—
溶媒Diethyl EtherHCID 3283—
溶媒HexaneHCID 8058—
生成物(6-Bromo-4-methylpyridin-3-yl)(2,5-difluorophenyl)methanolHCID 5773641434%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08114886B2
出典データセットuspto-grants-2012_02
ORD IDord-34104e0a00724cbab9759f5380b05975
出典メモuspto-grants-2012_02