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HRID 1246549생성일: 2026년 10월 23일

Pyridine → (3-Bromothien-2-yl) (3-methoxyphenyl)methanone oxime

https://huagongshe.com/ko/reaction/1246549

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물DichloromethaneHCID 6344—
반응물Hydroxyamine hydrochlorideHCID 443297—
반응물(3-Bromothien-2-yl) (3-methoxyphenyl)methanoneHCID 21915416—
용매HexaneHCID 8058—
생성물(3-Bromothien-2-yl) (3-methoxyphenyl)methanone oximeHCID 7272731387%

반응 단계

Stir a mixture of (3-bromothiophen-2-yl)-(3-methoxyphenyl)methanone (7 g, 0.024 mol), hydroxylamine hydrochloride (3.09 g, 0.048 mol) and pyridine (40 mL) overnight at room temperature, and then heat the mixture (100° C.–105° C.) for four hours. TLC (dichloromethane) shows that the reaction is complete. Quench the reaction mixture with water and extract with ether (three times). Wash the ether phase with HCl (3N) and water, dry (MgSO4), filter and concentrate to yield an oil that solidifies. Recrystallize the solid from ether:hexane to obtain the title compound (6.4 g, 87% Yield), m.p. 102–103° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07125903B1
출처 데이터셋uspto-grants-2006_10
ORD IDord-57b78ac06de9427ea6e74f79c1c384e6
출처 메모uspto-grants-2006_10