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HRID 1048356作成日:2026年10月25日

3-Chlorophenylacetic acid → 2-(3-Chlorophenyl)-1-(5-chloropyridin-2-yl)ethanone

https://huagongshe.com/reaction/1048356

反応式

関与物質

役割名称HCID仕込み量
反応物3-Chlorophenylacetic acidHCID 15879—
反応物Ammonium ChlorideHCID 25517—
反応物Sodium bis(trimethylsilyl)amideHCID 2724254—
反応物Methyl 5-chloropyridine-2-carboxylateHCID 11298216—
溶媒TetrahydrofuranHCID 8028—
生成物2-(3-Chlorophenyl)-1-(5-chloropyridin-2-yl)ethanoneHCID 58573659—

反応条件

温度-78 °C

反応手順

To a solution of 3-chlorophenylacetic acid (326.5 g, 1.91 mol, 0.95 eq) in THF (1.82 L) at −78° C. was slowly added NaHMDS (1M solution in THF, 3.82 L, 3.82 mol, 2 eq) over 2 h 45 min while keeping the temperature below −65° C. After the addition was complete, the reaction mixture was stirred for 30 min at −78° C. A solution of methyl 5-chloropicolinate (326.5 g, 1.91 mol, Example 121, Step A) in THF (0.9 L) was added to the above solution at −78° C. over 30 min. The reaction was stirred for another 1 h and then allowed to warm to ambient temperature overnight. The reaction mixture was slowly transferred into a sat. aq. ammonium chloride solution (4 L), extracted with ethyl acetate (2×8 L), and then the combined organic layers were dried over Na2SO4, filtered and the filtrate was concentrated. Purification of the residue by flash chromatography on silica gel (eluent: DCM) provided the title compound as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08569341B2
出典データセットuspto-grants-2013_10
ORD IDord-48ad3ccb90394ead8f4aedd45dcc4b63
出典メモuspto-grants-2013_10