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HRID 273323作成日:2026年10月27日

Diisopropylamine → 2-(5-Methoxypyridin-2-yl)-1-(3,4,5-trimethoxyphenyl)ethanone

https://huagongshe.com/reaction/273323

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylamineHCID 7912—
反応物TetrahydrofuranHCID 8028—
反応物HexaneHCID 8058—
反応物3,4,5-TrimethoxybenzonitrileHCID 15892—
反応物5-Methoxy-2-methylpyridineHCID 13358777—
反応物ButyllithiumHCID 178418339—
生成物2-(5-Methoxypyridin-2-yl)-1-(3,4,5-trimethoxyphenyl)ethanoneHCID 5295161775%

反応手順

n-BuLi in hexane (1.6 M, 7.6 mL, 11.9 mmol) was added dropwise to a solution of diisopropylamine (1.089 g, 10.9 mmol) in THF (25 mL) at −60 to −70° C. under N2. The mixture was stirred for 10 min. A solution of 5-methoxy-2-methyl-pyridine (1.274 g, 10.35 mmol) in THF (5 mL) was added dropwise to the above mixture. Stirring was continued for another 10 min and 3,4,5-trimethoxybenzonitrile (1.88 g, 9.74 mmol) in THF (5 mL) was added at −70° C. The mixture was stirred at −78° C. for 1 h and then allowed to warm to room temperature. Stirring was continued for another 2 h and the reaction mixture was poured into an ice-cold aqueous NH4Cl solution. The organic layer was separated and the aqueous phase was extracted with ether. The combined organic layers were extracted with a dilute HCl solution. The aqueous layer was washed with ether, neutralized with 10% aqueous NaOH, and extracted with ether. The organic layer was washed with water and dried. The residue was purified by chromatography eluting with CH2Cl2 to give 2-(5-methoxypyridin-2-yl)-1-(3,4,5-trimethoxyphenyl)ethanone (2.31 g, 75.0%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07456289B2
出典データセットuspto-grants-2008_11
ORD IDord-67840ed8090145518e38cfc7ab623d8b
出典メモuspto-grants-2008_11