돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 635849생성일: 2026년 10월 23일

Benzaldehyde → 2,3-Dimethyl-(2-phenyl-E-ethenyl)imidazo[2,1-b]thiazol-5-yl methanone

https://huagongshe.com/ko/reaction/635849

반응식

참여 물질

역할이름HCID투입량
반응물BenzaldehydeHCID 240—
반응물Sodium MethoxideHCID 10942334—
반응물2,3-Dimethylimidazo[2,1-b]thiazol-5-yl ethanoneHCID 21256445—
용매TetrahydrofuranHCID 8028—
생성물2,3-Dimethyl-(2-phenyl-E-ethenyl)imidazo[2,1-b]thiazol-5-yl methanoneHCID 21256502—

반응 단계

A solution of 1-(2,3-dimethylimidazo[2,1-b]thiazole-5-yl ethanone (See procedures from Preparation 6) (Formula D-1) (0.87 g) in THF (25 mL) was treated with benzaldehyde (0.52 mL) and sodium methoxide (0.11 g). After 18 hours trace 1-(2,3-dimethylimidazo[2,1-b]thiazol-5-yl ethanone remained and additional benzaldehyde (0.2 mL) was added. After an additional 2.5 hours the reaction was diluted with ice water and precipitated 2,3-Dimethyl-(2-phenyl-E-ethenyl)imidazo[2,1-b]thiazol-5-yl methanone (FIG. D-2) (1.03 g) was filtered. Crystallization from isopropanol solution gave pure 2,3-Dimethyl-(2-phenyl-E-ethenyl)imidazo[2,1-b]thiazol-5-yl methanone (FIG. D-2), m.p. 189-190°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06191124B1
출처 데이터셋uspto-grants-2001_02
ORD IDord-efe77d216995480d8840f4818aead038
출처 메모uspto-grants-2001_02