4-(((tert-butyl)dimethylsilyl)oxy)-2-(furan-2-yl)-5-(4-nitrophenyl)thiazole

Base Information

Chemical Name:4-(((tert-butyl)dimethylsilyl)oxy)-2-(furan-2-yl)-5-(4-nitrophenyl)thiazole
CAS No.:1417902-12-5
Molecular Formula:C₁₉H₂₂N₂O₄SSi
Molecular Weight:402.546
Hs Code.:

Synonyms:4-(((tert-butyl)dimethylsilyl)oxy)-2-(furan-2-yl)-5-(4-nitrophenyl)thiazole

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Chemical Property of 4-(((tert-butyl)dimethylsilyl)oxy)-2-(furan-2-yl)-5-(4-nitrophenyl)thiazole

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Technology Process of 4-(((tert-butyl)dimethylsilyl)oxy)-2-(furan-2-yl)-5-(4-nitrophenyl)thiazole

There total 3 articles about 4-(((tert-butyl)dimethylsilyl)oxy)-2-(furan-2-yl)-5-(4-nitrophenyl)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: 62.0%

: 1417902-08-9
2-(furan-2-yl)-5-(4-nitrophenyl)thiazol-4-ol

: 18162-48-6
tert-butyldimethylsilyl chloride

: 1417902-12-5
4-(((tert-butyl)dimethylsilyl)oxy)-2-(furan-2-yl)-5-(4-nitrophenyl)thiazole

Guidance literature:: With 1H-imidazole; In dichloromethane; for 24h; Inert atmosphere;
DOI:10.1016/j.tet.2012.12.016

Reference yield:

: 4691-72-9
ethyl α-bromo-p-nitrophenylacetate

: 1417902-12-5
4-(((tert-butyl)dimethylsilyl)oxy)-2-(furan-2-yl)-5-(4-nitrophenyl)thiazole

Guidance literature:: Multi-step reaction with 2 steps

1: toluene / 4 h / Inert atmosphere; Reflux

2: 1H-imidazole / dichloromethane / 24 h / Inert atmosphere

With 1H-imidazole; In dichloromethane; toluene; 1: |Hantzsch Thiazole Synthesis;
DOI:10.1016/j.tet.2012.12.016

Reference yield:

: 17572-09-7
2-furanthioamide

: 1417902-12-5
4-(((tert-butyl)dimethylsilyl)oxy)-2-(furan-2-yl)-5-(4-nitrophenyl)thiazole

Guidance literature:: Multi-step reaction with 2 steps

1: toluene / 4 h / Inert atmosphere; Reflux

2: 1H-imidazole / dichloromethane / 24 h / Inert atmosphere

With 1H-imidazole; In dichloromethane; toluene; 1: |Hantzsch Thiazole Synthesis;
DOI:10.1016/j.tet.2012.12.016