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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 981474생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/981474

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물5,6-Diphenyl-3(2H)-pyridazinoneHCID 150976—
반응물Methyl 9-bromononanoateHCID 554142—
용매WaterHCID 962—
생성물methyl 6-oxo-3,4-diphenyl-1(6H)-pyridazinenonanoateHCID 993184496.2%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04992439
출처 데이터셋uspto-grants-1991_02
ORD IDord-2de90a7cd6704c34a10f3605c9ea7f9c
출처 메모uspto-grants-1991_02