5-(3-hydroxyl-1-triphenylmethylthio-1-propyl)-1-methyl-1H-1,2,4-triazole

Base Information

Chemical Name:5-(3-hydroxyl-1-triphenylmethylthio-1-propyl)-1-methyl-1H-1,2,4-triazole
CAS No.:153851-61-7
Molecular Formula:C₂₅H₂₅N₃OS
Molecular Weight:415.559
Hs Code.:

Synonyms:5-(3-hydroxyl-1-triphenylmethylthio-1-propyl)-1-methyl-1H-1,2,4-triazole

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Chemical Property of 5-(3-hydroxyl-1-triphenylmethylthio-1-propyl)-1-methyl-1H-1,2,4-triazole

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Technology Process of 5-(3-hydroxyl-1-triphenylmethylthio-1-propyl)-1-methyl-1H-1,2,4-triazole

There total 3 articles about 5-(3-hydroxyl-1-triphenylmethylthio-1-propyl)-1-methyl-1H-1,2,4-triazole 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%

: 153851-60-6
5-(3-tert-butyldimethylsilyloxy-1-triphenylmethylthio-1-propyl)-1-methyl-1H-1,2,4-triazole

: 153851-61-7
5-(3-hydroxyl-1-triphenylmethylthio-1-propyl)-1-methyl-1H-1,2,4-triazole

Guidance literature:: With tetrabutyl ammonium fluoride; acetic acid; In tetrahydrofuran; at 0 - 20 ℃; for 8h;
DOI:10.7164/antibiotics.46.1866

Reference yield:

: 153851-58-2
5-(3-tert-butyldimethylsilyloxy-1-hydroxypropyl)-1-methyl-1H-1,2,4-triazole

: 153851-61-7
5-(3-hydroxyl-1-triphenylmethylthio-1-propyl)-1-methyl-1H-1,2,4-triazole

Guidance literature:: Multi-step reaction with 3 steps

1: 414 mg / triethylamine / CH₂Cl₂ / 0.67 h

2: 1.) n-butyllithium / 1.) THF, hexane, 0 deg C, 5 min, 2.) THF, hexane, RT, 16 h

3: 100 percent / AcOH, tetrabutylammonium fluoride / tetrahydrofuran / 8 h / 0 - 20 °C

With n-butyllithium; tetrabutyl ammonium fluoride; acetic acid; triethylamine; In tetrahydrofuran; dichloromethane;
DOI:10.7164/antibiotics.46.1866

Reference yield:

: 153851-59-3
Methanesulfonic acid 3-(tert-butyl-dimethyl-silanyloxy)-1-(2-methyl-2H-[1,2,4]triazol-3-yl)-propyl ester

: 153851-61-7
5-(3-hydroxyl-1-triphenylmethylthio-1-propyl)-1-methyl-1H-1,2,4-triazole

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) n-butyllithium / 1.) THF, hexane, 0 deg C, 5 min, 2.) THF, hexane, RT, 16 h

2: 100 percent / AcOH, tetrabutylammonium fluoride / tetrahydrofuran / 8 h / 0 - 20 °C

With n-butyllithium; tetrabutyl ammonium fluoride; acetic acid; In tetrahydrofuran;
DOI:10.7164/antibiotics.46.1866