戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 370027作成日:2026年10月26日

Water → 4-amino-3-chloro-5-methoxyiminomethyl-N-(3-chloro-1-ethyl-1-methyl-2-oxopropyl)benzamide

https://huagongshe.com/reaction/370027

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium BicarbonateHCID 516892—
反応物3-Amino-1-chloro-3-methylpentan-2-one hydrochlorideHCID 18372002—
反応物4-Amino-3-chloro-5-methoxyiminomethylbenzoyl chlorideHCID 54454051—
溶媒DichloromethaneHCID 6344—
溶媒Ethyl AcetateHCID 8857—
生成物4-amino-3-chloro-5-methoxyiminomethyl-N-(3-chloro-1-ethyl-1-methyl-2-oxopropyl)benzamideHCID 5410187474%

反応手順

In a 5-liter three-necked round bottomed flask was placed 93 g of 3-amino-1-chloro-3-methyl-2-pentanone hydrochloride and 885 mL of water. To the resulting solution were added 138.6 g of sodium bicarbonate followed by 500 mL of ethyl acetate. To the resulting well-stirred mixture was added 123.5 g of 4-amino-3-chloro-5-methoxyiminomethylbenzoyl chloride dissolved in 1000 mL of ethyl acetate at room temperature over a period of 50 minutes. After the addition was complete the reaction mixture was stirred at room temperature for 1 hour. The two phases were separated and the organic layer was washed with water (2×500 mL), brine (1×500 mL), dried over anhydrous magnesium sulfate and the solvent eliminated in a rotary evaporator yielding the crude product as a brown oil. This oil was passed through a short silica gel column using methylene chloride as elution solvent. Evaporation of the solvent yielded 133.3 g of the expected 4-amino-3-chloro-5-methoxyiminomethyl-N-(3-chloro-1-ethyl-1-methyl-2-oxopropyl)benzamide as an off-white solid (mp 140-141° C.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06140362
出典データセットuspto-grants-2000_10
ORD IDord-59165edfe56b4de19f2fe17a580efdb8
出典メモuspto-grants-2000_10