3-phenyl-2-(1,1,2,2-tetrafluoroethoxy)benzo[4,5]imidazo[2,1-b]thiazole

Base Information

Chemical Name:3-phenyl-2-(1,1,2,2-tetrafluoroethoxy)benzo[4,5]imidazo[2,1-b]thiazole
CAS No.:1369762-03-7
Molecular Formula:C₁₇H₁₀F₄N₂OS
Molecular Weight:366.339
Hs Code.:

Synonyms:3-phenyl-2-(1,1,2,2-tetrafluoroethoxy)benzo[4,5]imidazo[2,1-b]thiazole

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Chemical Property of 3-phenyl-2-(1,1,2,2-tetrafluoroethoxy)benzo[4,5]imidazo[2,1-b]thiazole

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Technology Process of 3-phenyl-2-(1,1,2,2-tetrafluoroethoxy)benzo[4,5]imidazo[2,1-b]thiazole

There total 6 articles about 3-phenyl-2-(1,1,2,2-tetrafluoroethoxy)benzo[4,5]imidazo[2,1-b]thiazole which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 91.0%

: 1369762-02-6
3-chloro-3-phenyl-2-(1,1,2,2-tetrafluoroethoxy)-2,3-dihydro-benzo[4,5]imidazo[2,1-b]thiazole

: 1369762-03-7
3-phenyl-2-(1,1,2,2-tetrafluoroethoxy)benzo[4,5]imidazo[2,1-b]thiazole

Guidance literature:: With potassium hydroxide; In ethanol; at 25 ℃; for 1h;
DOI:10.1016/j.jfluchem.2012.01.005

Reference yield:

: 1369761-86-3
1-phenyl-1,1-dimethoxy-2-(1,1,2,2-tetrafluoroethoxy)ethane

: 1369762-03-7
3-phenyl-2-(1,1,2,2-tetrafluoroethoxy)benzo[4,5]imidazo[2,1-b]thiazole

Guidance literature:: Multi-step reaction with 5 steps

1: hydrogenchloride; water / 1,4-dioxane / 18 h / 60 °C

2: N-Bromosuccinimide; toluene-4-sulfonic acid / tetrachloromethane / 24 h / 60 °C

3: 1,4-dioxane / 18 h / 90 °C

4: thionyl chloride / dichloromethane / 1 h / Reflux

5: potassium hydroxide / ethanol / 1 h / 25 °C

With hydrogenchloride; N-Bromosuccinimide; thionyl chloride; water; toluene-4-sulfonic acid; potassium hydroxide; In 1,4-dioxane; tetrachloromethane; ethanol; dichloromethane; 3: Hantzsch type cyclization;
DOI:10.1016/j.jfluchem.2012.01.005

Reference yield:

: 1369761-88-5
phenyl[(1,1,2,2-tetrafluoroethoxy)methyl]ketone

: 1369762-03-7
3-phenyl-2-(1,1,2,2-tetrafluoroethoxy)benzo[4,5]imidazo[2,1-b]thiazole

Guidance literature:: Multi-step reaction with 4 steps

1: N-Bromosuccinimide; toluene-4-sulfonic acid / tetrachloromethane / 24 h / 60 °C

2: 1,4-dioxane / 18 h / 90 °C

3: thionyl chloride / dichloromethane / 1 h / Reflux

4: potassium hydroxide / ethanol / 1 h / 25 °C

With N-Bromosuccinimide; thionyl chloride; toluene-4-sulfonic acid; potassium hydroxide; In 1,4-dioxane; tetrachloromethane; ethanol; dichloromethane; 2: Hantzsch type cyclization;
DOI:10.1016/j.jfluchem.2012.01.005