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HRID 1861213作成日:2026年10月25日

Pyridine → Ethyl 2-(2,4,5-trifluoro-3-methyl-6-nitrobenzoyl)-3-dimethylaminoacrylate

https://huagongshe.com/reaction/1861213

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Ethyl 3-(N,N-dimethylamino)acrylateHCID 121015—
反応物HCID 10610913HCID 10610913—
触媒Ethyl AcetateHCID 8857—
溶媒Ethyl AcetateHCID 8857—
生成物Ethyl 2-(2,4,5-trifluoro-3-methyl-6-nitrobenzoyl)-3-dimethylaminoacrylateHCID 72820967100.5%

反応条件

温度2.5 °C

反応手順

1.4 g (0.01 mol) of ethyl 3-dimethylaminoacrylate, 15 mg of ethyl acetate and 0.8 mg (0.01 mol) of pyridine were loaded and cooled below 5° C., and a liquid mixture of 3 g (0.01 mol) of 2,4,5-trifluoro-3-methyl-6-nitrobenzoyl chloride and 5 ml of ethyl acetate was added dropwise while the temperature was maintained at 0 to 5° C. The resulting mixture was stirred at 5° C. for 1 hour and then stirred at room temperature (25° C.) overnight (12 hours). The precipitated pyridine hydrochloride was filtered off, and the filtrate was concentrated under reduced pressure to give 3.62 g of ethyl 3-dimethylamino-2-(2,4,5-trifluoro-3-methyl-6-nitrobenzoyl)acrylate with a 87% purity (in terms of the percentage of the peak area in HPLC) as the residue.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06531624B1
出典データセットuspto-grants-2003_03
ORD IDord-d6e6b984bd674c68a064086fea3d5f04
出典メモuspto-grants-2003_03