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HRID 39304作成日:2026年10月23日

Methylhydrazine → 3-Chloro-6-(1-methylhydrazinyl)pyridazine

https://huagongshe.com/ja/reaction/39304

反応式

関与物質

役割名称HCID仕込み量
反応物MethylhydrazineHCID 6061—
反応物3,6-DichloropyridazineHCID 67331—
生成物3-Chloro-6-(1-methylhydrazinyl)pyridazineHCID 273581553.8%

反応手順

3,6-Dichloro-pyridazine (1 g, 6/5 mmol) was placed in a flask fitted with a water condenser and methylhydrazine (1.31 mL, 25 mmol) was added dropwise. An immediate exotherm was observed and methylhydrazine begins to reflux. When the reaction had subsided, the mixture was left for 16 hours, and the excess methylhydrazine was removed under reduced pressure. The cooled residue was stirred with aqueous sodium hydroxide solution (20 ml of 20%), and the resulting solution was extracted with ether (6×100 ml). The combined extracts were dried (K2CO3) and concentrated to give 427 mg of N-(6-Chloro-pyridazin-3-yl)-N-methyl-hydrazine.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524764B2
出典データセットuspto-grants-2013_09
ORD IDord-facf30b996f1484aaf341a84a6141e83
出典メモuspto-grants-2013_09