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HRID 981474作成日:2026年10月27日

Dimethylformamide → methyl 6-oxo-3,4-diphenyl-1(6H)-pyridazinenonanoate

https://huagongshe.com/reaction/981474

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物5,6-Diphenyl-3(2H)-pyridazinoneHCID 150976—
反応物Methyl 9-bromononanoateHCID 554142—
溶媒WaterHCID 962—
生成物methyl 6-oxo-3,4-diphenyl-1(6H)-pyridazinenonanoateHCID 993184496.2%

反応手順

Sodium hydride (840 mg of a 60% dispersion in oil, 20 mmol) was washed twice with hexanes, covered with DMF (25 mL) and 5,6-diphenyl-3(2H)-pyridazinone (4 g, 16 mmol), obtained according to P. Schmidt, et al., Helvetica Chim. Acta., 37, 134-140 (1954), added. After gas evolution had ceased, the mixture was stirred at room temperature for 30 minutes before adding methyl 9-bromononanoate (4.45 g, 18 mmol). The mixture was heated briefly to 110° C. to give a solution and then allowed to cool before being stirred at room temperature for 1 hour. The mixture was diluted with water and extracted with diethyl ether (3×). The combined extracts were washed with water, dried over sodium sulfate and concentrated to leave an oil. Chromatography on a column of silica gel afforded methyl 6-oxo-3,4-diphenyl-1(6H)-pyridazine nonanoate (6.44 g, 95%) as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04992439
出典データセットuspto-grants-1991_02
ORD IDord-2de90a7cd6704c34a10f3605c9ea7f9c
出典メモuspto-grants-1991_02