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HRID 414215作成日:2026年10月27日

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

https://huagongshe.com/reaction/414215

反応式

関与物質

役割名称HCID仕込み量
反応物Sulfuric AcidHCID 1118—
反応物Ammonium HydroxideHCID 14923—
反応物Ammonium PersulfateHCID 62648—
反応物3,6-DichloropyridazineHCID 67331—
反応物2,2-Dichloro-1-methylcyclopropanecarboxylic acidHCID 102621—
触媒Silver NitrateHCID 24470—
溶媒WaterHCID 962—
生成物3,6-Dichloro-4-(2,2-dichloro-1-methylcyclopropyl)pyridazineHCID 14349836—

反応手順

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°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04791110
出典データセットuspto-grants-1988_12
ORD IDord-8520f1702dc845749ca8922d1996b242
出典メモuspto-grants-1988_12