(E)-3-{3-[2-(4-Trifluoromethyl-phenyl)-oxazol-4-ylmethoxy]-phenyl}-but-2-en-1-ol

Base Information

Chemical Name:(E)-3-{3-[2-(4-Trifluoromethyl-phenyl)-oxazol-4-ylmethoxy]-phenyl}-but-2-en-1-ol
CAS No.:1026486-35-0
Molecular Formula:C₂₁H₁₈F₃NO₃
Molecular Weight:389.374
Hs Code.:

Synonyms:(E)-3-{3-[2-(4-Trifluoromethyl-phenyl)-oxazol-4-ylmethoxy]-phenyl}-but-2-en-1-ol

Suppliers and Price of (E)-3-{3-[2-(4-Trifluoromethyl-phenyl)-oxazol-4-ylmethoxy]-phenyl}-but-2-en-1-ol

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (E)-3-{3-[2-(4-Trifluoromethyl-phenyl)-oxazol-4-ylmethoxy]-phenyl}-but-2-en-1-ol

Chemical Property:

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Technology Process of (E)-3-{3-[2-(4-Trifluoromethyl-phenyl)-oxazol-4-ylmethoxy]-phenyl}-but-2-en-1-ol

There total 6 articles about (E)-3-{3-[2-(4-Trifluoromethyl-phenyl)-oxazol-4-ylmethoxy]-phenyl}-but-2-en-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:

: 1026181-93-0
(E)-3-{3-[2-(4-Trifluoromethyl-phenyl)-oxazol-4-ylmethoxy]-phenyl}-but-2-enoic acid ethyl ester

: 1026486-35-0
(E)-3-{3-[2-(4-Trifluoromethyl-phenyl)-oxazol-4-ylmethoxy]-phenyl}-but-2-en-1-ol

Guidance literature:: With diisobutylaluminium hydride; In diethyl ether; at -78 ℃; for 0.5h;
DOI:10.1021/jm990476x

Reference yield:

: 121-71-1
3-Hydroxyacetophenone

: 1026486-35-0
(E)-3-{3-[2-(4-Trifluoromethyl-phenyl)-oxazol-4-ylmethoxy]-phenyl}-but-2-en-1-ol

Guidance literature:: Multi-step reaction with 3 steps

1.1: K₂CO₃ / dimethylformamide / 10 h / 65 °C

2.1: NaH / toluene / 1 h

2.2: toluene; tetrahydrofuran / 48 h

3.1: DIBAL / diethyl ether / 0.5 h / -78 °C

With sodium hydride; diisobutylaluminium hydride; potassium carbonate; In diethyl ether; N,N-dimethyl-formamide; toluene; 1.1: Alkylation / 2.1: Metallation / 2.2: Condensation / 3.1: Reduction;
DOI:10.1021/jm990476x

Reference yield:

: 1891-90-3
p-trifluoromethylbenzamide

: 1026486-35-0
(E)-3-{3-[2-(4-Trifluoromethyl-phenyl)-oxazol-4-ylmethoxy]-phenyl}-but-2-en-1-ol

Guidance literature:: Multi-step reaction with 5 steps

1.1: NaHCO₃ / 1,2-dichloro-ethane

2.1: SOCl₂

3.1: K₂CO₃ / dimethylformamide / 10 h / 65 °C

4.1: NaH / toluene / 1 h

4.2: toluene; tetrahydrofuran / 48 h

5.1: DIBAL / diethyl ether / 0.5 h / -78 °C

With thionyl chloride; sodium hydride; diisobutylaluminium hydride; sodium hydrogencarbonate; potassium carbonate; In diethyl ether; 1,2-dichloro-ethane; N,N-dimethyl-formamide; toluene; 1.1: Alkylation / 2.1: Cyclization / 3.1: Alkylation / 4.1: Metallation / 4.2: Condensation / 5.1: Reduction;
DOI:10.1021/jm990476x