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HRID 279848作成日:2026年10月26日

2-Amino-5-chloro-2'-fluorobenzophenone → 2-{[2-Amino-5-chloro-alpha-(2-fluorophenyl)benzylidene]amino}ethanol

https://huagongshe.com/reaction/279848

反応式

関与物質

役割名称HCID仕込み量
反応物2-Amino-5-chloro-2'-fluorobenzophenoneHCID 69912—
反応物Sodium BicarbonateHCID 516892—
反応物2-Methylimidazole hydrochlorideHCID 521629—
溶媒EthanolamineHCID 700—
生成物2-{[2-Amino-5-chloro-alpha-(2-fluorophenyl)benzylidene]amino}ethanolHCID 23322779—

反応手順

A mixture of 40 g of 2-methylimidazole hydrochloride and of 90 g of 2-amino-5-chloro-2'-fluoro-benzophenone in 240 ml of ethanolamine is heated at 135° for 2 hours. After cooling, the reaction mixture is poured into an aqueous sodium bicarbonate solution. The mixture is extracted with ether, the organic phase is washed repeatedly with water and is dried over sodium sulphate, and the solvent is evaporated to dryness. The residual oil is chromatographed on a silica column, elution being carried out with a 50/50 mixture of cyclohexane and ethyl acetate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04587245
出典データセットuspto-grants-1986_05
ORD IDord-eea19af2b3f74012a5225b25d3936404
出典メモuspto-grants-1986_05