2-(1-Trityl-1H-imidazol-4-yl)ethanol

Base Information

• Chemical Name: 2-(1-Trityl-1H-imidazol-4-yl)ethanol
• CAS No.: 127607-62-9
• Molecular Formula: C24H22N2O
• Molecular Weight: 354.451
• DSSTox Substance ID: DTXSID40443578
• Wikidata: Q82261468
• Mol file: 127607-62-9.mol

Synonyms:2-(1-Trityl-1H-imidazol-4-yl)ethanol;127607-62-9;2-(1-tritylimidazol-4-yl)ethanol;1H-Imidazole-4-ethanol, 1-(triphenylmethyl)-;1-triphenylmethyl-4-(2-hydroxyethyl)-1H-imidazole;SCHEMBL1041048;DTXSID40443578;PGCGACBWMXEHHA-UHFFFAOYSA-N;2-(1-trityl-1H-imidazol-4-yl)-ethanol;AS-49994;2-(1-triphenylmethyl-1H-imidazol-4-yl)ethanol;O10448;1-(triphenylmethyl)-4-(2-hydroxyethyl)imidazole;A889171;2-[1-(triphenylmethyl)-1H-imidazol-4-yl]ethan-1-ol

Chemical Property of 2-(1-Trityl-1H-imidazol-4-yl)ethanol

Chemical Property:

• PSA: 38.05000
• LogP: 4.25810
• XLogP3: 4.4
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 6
• Exact Mass: 354.173213330
• Heavy Atom Count: 27
• Complexity: 390

Purity/Quality:

97% ^*data from raw suppliers

2-(1-Trityl-1H-imidazol-4-yl)ethanol ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)C(C2=CC=CC=C2)(C3=CC=CC=C3)N4C=C(N=C4)CCO

Technology Process of 2-(1-Trityl-1H-imidazol-4-yl)ethanol

There total 8 articles about 2-(1-Trityl-1H-imidazol-4-yl)ethanol 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: 87.0%

1-triphenylmethyl-4-imidazolyl-acetic acid (168632-03-9) → 1-triphenylmethyl-4-(2-hydroxyethyl)-1H-imidazole (127607-62-9)

Guidance literature:

With diborane; In tetrahydrofuran; at 0 - 25 ℃;

Reference yield: 69.0%

trityl chloride (76-83-5) + 2-(1H-imidazol-4-yl)ethanol*HCl → 1-triphenylmethyl-4-(2-hydroxyethyl)-1H-imidazole (127607-62-9)

Guidance literature:

With triethylamine; In N,N-dimethyl-formamide; at 20 ℃; for 2h;

DOI:10.1021/jm960138l

Reference yield: 59.0%

1-(Triphenylmethyl)-1H-imidazole-4-ethanoic acid ethyl ester → 1-triphenylmethyl-4-(2-hydroxyethyl)-1H-imidazole (127607-62-9)

Guidance literature:

With lithium aluminium tetrahydride; In tetrahydrofuran; at 25 ℃; Inert atmosphere;

upstream raw materials:

trityl chloride

1-triphenylmethyl-4-imidazolyl-acetic acid

imidazole-4-acetic acid hydrochloride

2-(1H-imidazol-4-yl)ethanol

Downstream raw materials:

2-[3-(4'-fluorobiphenyl-2-ylmethyl)-3H-imidazol-4-yl]ethanol

5-(2-chloroethyl)-1-(4'-fluorobiphenyl-2-ylmethyl)-1H-imidazole

3-bromo-4-(6,7-dihydro-5H-pyrrolo[1,2-c]imidazol-5-yl)benzonitrile