2-{(S)-1-[5-[(S)-1-(2-Hydroxy-ethoxy)-ethyl]-2-(4-methoxy-benzyl)-2H-[1,2,4]triazol-3-yl]-ethoxy}-ethanol

Base Information

Chemical Name:2-{(S)-1-[5-[(S)-1-(2-Hydroxy-ethoxy)-ethyl]-2-(4-methoxy-benzyl)-2H-[1,2,4]triazol-3-yl]-ethoxy}-ethanol
CAS No.:164061-56-7
Molecular Formula:C₁₈H₂₇N₃O₅
Molecular Weight:365.429
Hs Code.:

Synonyms:2-{(S)-1-[5-[(S)-1-(2-Hydroxy-ethoxy)-ethyl]-2-(4-methoxy-benzyl)-2H-[1,2,4]triazol-3-yl]-ethoxy}-ethanol

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Chemical Property of 2-{(S)-1-[5-[(S)-1-(2-Hydroxy-ethoxy)-ethyl]-2-(4-methoxy-benzyl)-2H-[1,2,4]triazol-3-yl]-ethoxy}-ethanol

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Technology Process of 2-{(S)-1-[5-[(S)-1-(2-Hydroxy-ethoxy)-ethyl]-2-(4-methoxy-benzyl)-2H-[1,2,4]triazol-3-yl]-ethoxy}-ethanol

There total 4 articles about 2-{(S)-1-[5-[(S)-1-(2-Hydroxy-ethoxy)-ethyl]-2-(4-methoxy-benzyl)-2H-[1,2,4]triazol-3-yl]-ethoxy}-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:

: 1-(4-Methoxy-benzyl)-3,5-bis-{(S)-1-[2-(tetrahydro-pyran-2-yloxy)-ethoxy]-ethyl}-1H-[1,2,4]triazole

: 164061-56-7
2-{(S)-1-[5-[(S)-1-(2-Hydroxy-ethoxy)-ethyl]-2-(4-methoxy-benzyl)-2H-[1,2,4]triazol-3-yl]-ethoxy}-ethanol

Guidance literature:: With hydrogenchloride; In methanol; for 5h; Yield given; Heating;
DOI:10.1055/s-1994-25644

Reference yield:

: 111853-55-5
(S,S)-3,5-bis(1-hydroxyethyl)-1H-1,2,4-triazole

: 164061-56-7
2-{(S)-1-[5-[(S)-1-(2-Hydroxy-ethoxy)-ethyl]-2-(4-methoxy-benzyl)-2H-[1,2,4]triazol-3-yl]-ethoxy}-ethanol

Guidance literature:: Multi-step reaction with 3 steps

1: 80 percent / K₂CO₃, tetrabutylammonium hydrogen sulfate / acetonitrile / 3 h / 60 °C

2: 1.) NaH, (60percent in min. oil) / 1.) THF, 70 deg C, 30 min, 2.) THF, 70 deg C, 24 h

3: conc. HCl / methanol / 5 h / Heating

With hydrogenchloride; tetra(n-butyl)ammonium hydrogensulfate; sodium hydride; potassium carbonate; In methanol; acetonitrile;
DOI:10.1055/s-1994-25644

Reference yield:

: 824-94-2
p-methoxybenzyl chloride

: 164061-56-7
2-{(S)-1-[5-[(S)-1-(2-Hydroxy-ethoxy)-ethyl]-2-(4-methoxy-benzyl)-2H-[1,2,4]triazol-3-yl]-ethoxy}-ethanol

Guidance literature:: Multi-step reaction with 3 steps

1: 80 percent / K₂CO₃, tetrabutylammonium hydrogen sulfate / acetonitrile / 3 h / 60 °C

2: 1.) NaH, (60percent in min. oil) / 1.) THF, 70 deg C, 30 min, 2.) THF, 70 deg C, 24 h

3: conc. HCl / methanol / 5 h / Heating

With hydrogenchloride; tetra(n-butyl)ammonium hydrogensulfate; sodium hydride; potassium carbonate; In methanol; acetonitrile;
DOI:10.1055/s-1994-25644