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HRID 1073863作成日:2026年10月27日

Ammonium Chloride → 1-(2-Methoxyphenyl)-3-methyl-1-(2-pyridyl)-2-buten-1-ol

https://huagongshe.com/reaction/1073863

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1-Bromo-2-methyl-1-propeneHCID 98560—
反応物2-(2-Methoxybenzoyl)pyridineHCID 603942—
反応物MagnesiumHCID 5462224—
溶媒TetrahydrofuranHCID 8028—
生成物1-(2-Methoxyphenyl)-3-methyl-1-(2-pyridyl)-2-buten-1-olHCID 1989559660.7%

反応手順

43.84 g of 1-bromo-2-methylprop-1-ene in 150 ml of tetrahydrofuran were added dropwise to 9.8 g of magnesium in 50 ml of tetrahydrofuran while heating at reflux. After 1 hour the mixture was allowed to cool to room temperature, whereupon 47.7 g of 2-methoxyphenyl 2-pyridyl ketone in 200 ml of tetrahydrofuran were added slowly. After stirring for 2 hours at room temperature 200 ml of saturated ammonium chloride were added and the mixture was extracted with ethyl acetate. The organic extract was dried over sodium sulphate and evaporated. The residue was chromatographed on silica gel using ethyl acetate/petroleum ether (1:6) followed by ethyl acetate/petroleum ethyl (1:4) for the elution to yield 36.6 g of 1-(2-methoxyphenyl)-3-methyl-1-(2-pyridyl) -2-buten-1-ol in the form of an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04971982
出典データセットuspto-grants-1990_11
ORD IDord-4ac034a99f454a8ab04abb67aaf2034c
出典メモuspto-grants-1990_11