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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 602566생성일: 2026년 10월 26일

Iodoethane → 9-Ethyl-3-methyl[1,3]thiazolo[3,2-a]benzimidazol-9-ium iodide

https://huagongshe.com/reaction/602566

반응식

참여 물질

역할이름HCID투입량
반응물IodoethaneHCID 6340—
반응물3-Methyl[1,3]thiazolo[3,2-a]benzimidazoleHCID 828285—
용매AcetoneHCID 180—
생성물9-Ethyl-3-methyl[1,3]thiazolo[3,2-a]benzimidazol-9-ium iodideHCID 45027577—

반응 단계

153 mg of 3-methyl[1,3]thiazolo[3,2-a]benzimidazole were solubilised in acetone (5 mL). Then 328 μl, (5 eq) of iodoethane were added and the solution stirred under reflux. After 18 h, 9-ethyl-3-methyl[1,3]thiazolo[3,2-a]benzimidazol-9-ium iodide was recovered as a white powder (267 mg, 96%) by filtration. Mp 268° C.; 1H NMR (300 MHz, MeOD) δ=1.64 (3H, t, J=7.3, CH3), 2.95 (3H, d, J=CH3), 4.66 (2H, q, J=7.3, CH2), 7.37 (1H, q, J=1.3, H5), 7.66-7.81 (2H, m, Ar), 8.01-8.04 (1H, m, Ar), 8.27-8.30 (1H, m, Ar); 13C NMR (75 MHz, MeOD) δ=13.21, 14.25, 43.61, 112.19, 113.66, 114.93, 126.26, 128.32, 129.05, 135.29, 137.28, 155.62.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07906541B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-d2f94d58b9654daab1d4639f5ff291d5
출처 메모uspto-grants-2011_03