(1S)-1-{3-[5-fluoro-3-(trifluoromethyl)phenyl](1,2,4-oxadiazol-5-yl)}ethan-1-ol

Base Information

Chemical Name:(1S)-1-{3-[5-fluoro-3-(trifluoromethyl)phenyl](1,2,4-oxadiazol-5-yl)}ethan-1-ol
CAS No.:1050239-70-7
Molecular Formula:C₁₁H₈F₄N₂O₂
Molecular Weight:276.19
Hs Code.:

Synonyms:(1S)-1-{3-[5-fluoro-3-(trifluoromethyl)phenyl](1,2,4-oxadiazol-5-yl)}ethan-1-ol

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Chemical Property of (1S)-1-{3-[5-fluoro-3-(trifluoromethyl)phenyl](1,2,4-oxadiazol-5-yl)}ethan-1-ol

Chemical Property:

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Technology Process of (1S)-1-{3-[5-fluoro-3-(trifluoromethyl)phenyl](1,2,4-oxadiazol-5-yl)}ethan-1-ol

There total 4 articles about (1S)-1-{3-[5-fluoro-3-(trifluoromethyl)phenyl](1,2,4-oxadiazol-5-yl)}ethan-1-ol 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:

: 1050239-68-3
(1S)-1-{3-[5-fluoro-3-(trifluoromethyl)phenyl](1,2,4-oxadiazol-5-yl)}ethyl acetate

: 1050239-70-7
(1S)-1-{3-[5-fluoro-3-(trifluoromethyl)phenyl](1,2,4-oxadiazol-5-yl)}ethan-1-ol

Guidance literature:: With water; potassium carbonate; In methanol; at -15 - 20 ℃; for 1.33333h;

Reference yield:

: 885956-71-8
3-fluoro-N'-hydroxy-5-(trifluoromethyl)benzimidamide

: 1050239-70-7
(1S)-1-{3-[5-fluoro-3-(trifluoromethyl)phenyl](1,2,4-oxadiazol-5-yl)}ethan-1-ol

Guidance literature:: Multi-step reaction with 3 steps

1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 2 h / -78 - 20 °C

2: tetrabutyl ammonium fluoride / tetrahydrofuran / 3 h / 0 °C

3: water; potassium carbonate / methanol / 1.33 h / -15 - 20 °C

With tetrabutyl ammonium fluoride; water; potassium carbonate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol;

Reference yield:

: 1050239-66-1
2-amino-2-[3-fluoro-5-(trifluoromethyl)phenyl]-1-azavinyl (2S)-2-acetyloxypropanoate

: 1050239-70-7
(1S)-1-{3-[5-fluoro-3-(trifluoromethyl)phenyl](1,2,4-oxadiazol-5-yl)}ethan-1-ol

Guidance literature:: Multi-step reaction with 2 steps

1: tetrabutyl ammonium fluoride / tetrahydrofuran / 3 h / 0 °C

2: water; potassium carbonate / methanol / 1.33 h / -15 - 20 °C

With tetrabutyl ammonium fluoride; water; potassium carbonate; In tetrahydrofuran; methanol;