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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 39304생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물MethylhydrazineHCID 6061—
반응물3,6-DichloropyridazineHCID 67331—
생성물3-Chloro-6-(1-methylhydrazinyl)pyridazineHCID 273581553.8%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524764B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-facf30b996f1484aaf341a84a6141e83
출처 메모uspto-grants-2013_09