1H-Imidazole-1-carboxylic acid, 3-phenylpropyl ester

Base Information

Chemical Name:1H-Imidazole-1-carboxylic acid, 3-phenylpropyl ester
CAS No.:170895-01-9
Molecular Formula:C13H14N2O2
Molecular Weight:230.266
Hs Code.:

Synonyms:

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Chemical Property of 1H-Imidazole-1-carboxylic acid, 3-phenylpropyl ester

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Technology Process of 1H-Imidazole-1-carboxylic acid, 3-phenylpropyl ester

There total 4 articles about 1H-Imidazole-1-carboxylic acid, 3-phenylpropyl ester 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: 100.0%

: 122-97-4
3-Phenyl-1-propanol

: 530-62-1
1,1'-carbonyldiimidazole

: 170895-01-9
1-(3-phenylpropoxycarbonyl)-1H-imidazole

Guidance literature:: In dichloromethane; for 1h; Ambient temperature;
DOI:10.3987/COM-95-7048

Reference yield: 11.0%

: 122-97-4
3-Phenyl-1-propanol

: 530-62-1
1,1'-carbonyldiimidazole

: 102162-49-2
bis(3-phenylpropyl) carbonate

: 104-52-9
phenylpropyl chloride

: 170895-01-9
1-(3-phenylpropoxycarbonyl)-1H-imidazole

Guidance literature:: 3-Phenyl-1-propanol; 1,1'-carbonyldiimidazole; In acetonitrile; at 20 ℃; for 1h; Molecular sieve;

With dibenzo-18-crown-6; potassium chloride; toluene-4-sulfonic acid; In acetonitrile; for 24h; Reflux; Molecular sieve;
DOI:10.1016/j.tetlet.2015.01.098

Reference yield:

: 122-97-4
3-Phenyl-1-propanol

: 530-62-1
1,1'-carbonyldiimidazole

: 637-59-2
1-Bromo-3-phenylpropane

: 170895-01-9
1-(3-phenylpropoxycarbonyl)-1H-imidazole

Guidance literature:: 3-Phenyl-1-propanol; 1,1'-carbonyldiimidazole; In acetonitrile; at 20 ℃; for 1h; Molecular sieve;

With Pyridine hydrobromide; In acetonitrile; Solvent; Reagent/catalyst; Reflux; Molecular sieve;
DOI:10.1016/j.tetlet.2015.01.098