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HRID 892501作成日:2026年10月26日

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

https://huagongshe.com/reaction/892501

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US05118694
出典データセットuspto-grants-1992_06
ORD IDord-59ac6b12727149d1a18c85ca6c5b4ed7
出典メモuspto-grants-1992_06