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HRID 723998作成日:2026年10月27日

Ethyl anisate → 2-(4-Chloro-2-pyridinyl)-1-(4-methoxyphenyl)ethanone

https://huagongshe.com/reaction/723998

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl anisateHCID 60979—
反応物4-Chloro-2-methylpyridineHCID 581392—
反応物Lithium HexamethyldisilazideHCID 2733832—
溶媒TetrahydrofuranHCID 8028—
生成物2-(4-Chloro-2-pyridinyl)-1-(4-methoxyphenyl)ethanoneHCID 21874054—

反応条件

温度45 °C

反応手順

To a cold (0° C.) solution of 4-chloro-2-picoline (10 g, 78.4 mmol) and ethyl 4-methoxybenzoate (14.1 g, 78.4 mmol) in tetrahydrofuran (100 mL) was added lithium bis(trimethylsilyl)amide (157 mL, 1.0 M in tetrahydrofuran, 157 mmol) dropwise via a pressure equalizing funnel over half an hour. Upon complete addition, the ice bath was removed and the resulting solution was heated at 45° C. for 15 hours. The mixture was cooled to room temperature, and the solution was concentrated. Methanol was added to quench the reaction, resulting in the formation of a yellow precipitate. The precipitate was collected by filtration and dried to give the product as a mixture of enol and ketone tautomers. MS m/z 262 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07141569B2
出典データセットuspto-grants-2006_11
ORD IDord-8158751891aa43319ab2d9f15e32c72a
出典メモuspto-grants-2006_11