4-(tert-butyl-diphenyl-silanyloxymethyl)-1-(2-methoxymethoxy-5-methyl-phenyl)-1H-imidazole

Base Information

• Chemical Name: 4-(tert-butyl-diphenyl-silanyloxymethyl)-1-(2-methoxymethoxy-5-methyl-phenyl)-1H-imidazole
• CAS No.: 854779-34-3
• Molecular Formula: C₂₉H₃₄N₂O₃Si
• Molecular Weight: 486.686
• Mol file: 854779-34-3.mol

Synonyms:4-(tert-butyl-diphenyl-silanyloxymethyl)-1-(2-methoxymethoxy-5-methyl-phenyl)-1H-imidazole

Chemical Property of 4-(tert-butyl-diphenyl-silanyloxymethyl)-1-(2-methoxymethoxy-5-methyl-phenyl)-1H-imidazole

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 4-(tert-butyl-diphenyl-silanyloxymethyl)-1-(2-methoxymethoxy-5-methyl-phenyl)-1H-imidazole

There total 1 articles about 4-(tert-butyl-diphenyl-silanyloxymethyl)-1-(2-methoxymethoxy-5-methyl-phenyl)-1H-imidazole 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:

2-bromo-1-(methoxymethoxy)-4-methylbenzene (104750-60-9) → 4-(tert-butyl-diphenyl-silanyloxymethyl)-1-(2-methoxymethoxy-5-methyl-phenyl)-1H-imidazole (854779-34-3)

Guidance literature:

Multi-step reaction with 2 steps

1.1: n-BuLi / diethyl ether / -70 °C

1.2: 65 percent / B(OMe)3 / diethyl ether

2.1: 75 percent / O₂ / [Cu(OH)TMEDA]2Cl₂ / CH₂Cl₂ / 20 °C

With n-butyllithium; oxygen; di-μ-hydroxo-bis[(N,N,N′,N′-tetramethylethylenediamine)copper(II)] chloride; In diethyl ether; dichloromethane;

DOI:10.1039/b311538k

Reference yield: 93.0%

4-(tert-butyl-diphenyl-silanyloxymethyl)-1-(2-methoxymethoxy-5-methyl-phenyl)-1H-imidazole (854779-34-3) → [1-(2-methoxymethoxy-5-methyl-phenyl)-1H-imidazol-4-yl]-methanol (854779-50-3)

Guidance literature:

With n-BuN-F; In tetrahydrofuran; at 20 ℃;

DOI:10.1039/b311538k

Reference yield:

4-(tert-butyl-diphenyl-silanyloxymethyl)-1-(2-methoxymethoxy-5-methyl-phenyl)-1H-imidazole (854779-34-3) → 6-{[[1-(2-methoxymethoxy-5-methyl-phenyl)-1H-imidazol-4-ylmethyl]-(1-methyl-1H-imidazol-2-ylmethyl)-amino]-methyl}-nicotinic acid (675583-74-1)

Guidance literature:

Multi-step reaction with 6 steps

1: 93 percent / n-BuN-F / tetrahydrofuran / 20 °C

2: 85 percent / MnO₂ / CHCl₃ / Heating

3: Et₃N / methanol

4: NaBH₄ / methanol

5: 61 percent / K₂CO₃ / acetonitrile / 20 °C

6: 86 percent / KOH / tetrahydrofuran / 20 °C

With manganese(IV) oxide; potassium hydroxide; sodium tetrahydroborate; n-BuN-F; potassium carbonate; triethylamine; In tetrahydrofuran; methanol; chloroform; acetonitrile;

DOI:10.1039/b311538k

upstream raw materials:

2-bromo-1-(methoxymethoxy)-4-methylbenzene

Downstream raw materials:

[1-(2-methoxymethoxy-5-methyl-phenyl)-1H-imidazol-4-yl]-methanol

1-(2-methoxymethoxy-5-methyl-phenyl)-1H-imidazole-4-carbaldehyde

[1-(2-methoxymethoxy-5-methyl-phenyl)-1H-imidazol-4-ylmethyl]-(1-methyl-1H-imidazol-2-ylmethyl)-amine

6-{[[1-(2-methoxymethoxy-5-methyl-phenyl)-1H-imidazol-4-ylmethyl]-(1-methyl-1H-imidazol-2-ylmethyl)-amino]-methyl}-nicotinic acid