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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 414215생성일: 2026년 10월 26일

Sulfuric Acid → 3,6-Dichloro-4-(2,2-dichloro-1-methylcyclopropyl)pyridazine

https://huagongshe.com/reaction/414215

반응식

참여 물질

역할이름HCID투입량
반응물Sulfuric AcidHCID 1118—
반응물Ammonium HydroxideHCID 14923—
반응물Ammonium PersulfateHCID 62648—
반응물3,6-DichloropyridazineHCID 67331—
반응물2,2-Dichloro-1-methylcyclopropanecarboxylic acidHCID 102621—
촉매Silver NitrateHCID 24470—
용매WaterHCID 962—
생성물3,6-Dichloro-4-(2,2-dichloro-1-methylcyclopropyl)pyridazineHCID 14349836—

반응 단계

A 3.5 g. portion of 3,6-dichloropyridazine was slurried with 4.0 g. of 2,2-dichloro-1-methylcyclopropanecarboxylic acid, 15 ml. of water, 3.4 g. of concentrated sulfuric acid in 20 ml. of water, and 4.0 g. of silver nitrate, and the mixture was heated to 65° with rapid stirring. To it was added 11.9 g. of ammonium persulfate in 20 ml. of water, over 20 minutes, while the temperature was held at 70°-76°. The mixture was stirred 15 minutes after the addition and cooled to 10°. Its pH was adjusted to 8.0 with ammonium hydroxide, and the water layer was then decanted off. The remaining solids were washed twice with 100 ml. portions of diethyl ether, and that ether was then used to extract the water layer. The organic layer was washed with 1N sodium hydroxide and with brine, and dried. The solvent was removed under vacuum, and the residue was purified by chromatography, eluting with 3:1 heptane:ethyl acetate. The product-containing fractions were combined and evaporated, and the residue was recrystallized from heptane, to obtain 0.52 g. of the desired product, m.p. 78°-79°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04791110
출처 데이터셋uspto-grants-1988_12
ORD IDord-8520f1702dc845749ca8922d1996b242
출처 메모uspto-grants-1988_12