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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 254254생성일: 2026년 10월 26일

Methanol → Methyl 6-chloropyridazine-3-carboxylate

https://huagongshe.com/reaction/254254

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Oxalyl chlorideHCID 65578—
반응물Sodium BicarbonateHCID 516892—
반응물6-chloropyridazine-3-carboxylic AcidHCID 6415762—
촉매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물Methyl 6-chloropyridazine-3-carboxylateHCID 1237980165%

반응 단계

Oxalyl chloride (1.14 mL, 13.09 mmol), was added dropwise to an ice-cold suspension of 6-chloro-pyridazine-3-carboxylic acid [(1.9 g, 11.9 mmol), J. Het. Chem. 29(6), 1583-92; 1992] in a mixture of dichloromethane (50 mL) and N,N-dimethylformamide (1 drop) and the mixture was stirred for 1 hour at room temperature. The reaction mixture was then evaporated under reduced pressure and the residue was diluted with dichloromethane (30 mL) and cooled to 0° C. Methanol (485 μL, 11.9 mmol) was added and the mixture was stirred at 0° C. for 1 hour. Sodium hydrogen carbonate solution was then added to the reaction mixture and the aqueous layer was separated and extracted with dichloromethane (×2). The combined organic solutions were washed with brine, dried over sodium sulfate and concentrated in vacuo to afford the title compound as a white solid in 65% yield, 1.33 g.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07875615B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-dda68b37c44b4ec6986e2b8cd03b57be
출처 메모uspto-grants-2011_01