1-(but-1-en-2-yl)-4-(trifluoromethyl)benzene

Base Information

Chemical Name:1-(but-1-en-2-yl)-4-(trifluoromethyl)benzene
CAS No.:326879-13-4
Molecular Formula:C₁₁H₁₁F₃
Molecular Weight:200.204
Hs Code.:

Synonyms:1-(but-1-en-2-yl)-4-(trifluoromethyl)benzene

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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 1-(but-1-en-2-yl)-4-(trifluoromethyl)benzene

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Technology Process of 1-(but-1-en-2-yl)-4-(trifluoromethyl)benzene

There total 1 articles about 1-(but-1-en-2-yl)-4-(trifluoromethyl)benzene 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%

: 711-33-1
4-trifluoromethyl propiophenone

: 326879-13-4
1-(but-1-en-2-yl)-4-(trifluoromethyl)benzene

Guidance literature:: Methyltriphenylphosphonium bromide; With potassium tert-butylate; In tetrahydrofuran; at 0 - 20 ℃; for 2h;

4-trifluoromethyl propiophenone; In tetrahydrofuran; at 0 - 20 ℃; for 2h;

Reference yield: 94.0%

: 326879-13-4
1-(but-1-en-2-yl)-4-(trifluoromethyl)benzene

: (E)-1-(but-2-en-2-yl)-4-(trifluoromethyl)benzene

Guidance literature:: With (PPO)FeCl₂; sodium triethylborohydride; In tetrahydrofuran; pentane; at 20 ℃; for 8h; stereoselective reaction; Inert atmosphere; Glovebox; Sealed tube; Schlenk technique;
DOI:10.1002/cjoc.202000492

Reference yield: 92.0%

: 201230-82-2
carbon monoxide

: 326879-13-4
1-(but-1-en-2-yl)-4-(trifluoromethyl)benzene

: (S)-3-(4-(trifluoromethyl)phenyl)pentanal

Guidance literature:: With (acetylacetonato)dicarbonylrhodium (l); (S,S)-YanPhos; hydrogen; In toluene; at 80 ℃; for 48h; under 3750.38 Torr; enantioselective reaction; Autoclave;
DOI:10.1021/jacs.8b00275