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HRID 50101作成日:2026年10月24日

Water → HCID 178500902、化合物

https://huagongshe.com/ja/reaction/50101

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物4-FluorobenzonitrileHCID 14517—
反応物Tin tetrachlorideHCID 24287—
反応物Methyl 4-methyl-3-oxopentanoateHCID 2759969—
溶媒TolueneHCID 1140—
溶媒HexaneHCID 8058—
溶媒Ethyl AcetateHCID 8857—
生成物HCID 178500902HCID 17850090281.5%

反応条件

温度80 °C

反応手順

22.53 g of methyl isobutyrylacetate (0.15 mol, concentration 96%) and 18.54 g of 4-fluorobenzonitrile (0.15 mol, concentration 98%) were dissolved in 150 ml of toluene and treated with 43.32 g of tin tetrachloride (0.165 mol, concentration 99%) at room temperature over the course of 12 min. After half an hour at room temperature, the mixture was heated to 80° C. After 3 h, the suspension was cooled to room temperature and treated with 150 ml of water. It was diluted with 100 ml of ethyl acetate and the phases were separated. After extraction of the aqueous phase with ethyl acetate (2×100 ml), the combined organic phases were washed with 100 ml of saturated aqueous sodium hydrogencarbonate solution, and 100 ml of 1N sodium hydroxide solution and dried over magnesium sulphate. After concentration in vacuo, 46.46 g of crude product were obtained in the form of a yellowish solid. The solid was dissolved in a mixture of 50 ml of n-hexane and 5 ml of toluene under reflux and filtered hot. The product precipitated from the filtrate on cooling. By filtering through a frit and washing the filter cake with 2×40 ml of n-hexane, 32.42 g of methyl 2-[1-amino-1-(4-fluorophenyl)methylene]-4-methyl-3-oxopentanoate were obtained in the form of a spectroscopically pure solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06710178B2
出典データセットuspto-grants-2004_03
ORD IDord-5e981c45b23e4be98159c0fce2877e2a
出典メモuspto-grants-2004_03