(R,E)-N-(4-cyano-1-phenylbut-3-en-2-yl)-2-(trifluoromethoxy)benzenesulfonamide

Base Information

Chemical Name:(R,E)-N-(4-cyano-1-phenylbut-3-en-2-yl)-2-(trifluoromethoxy)benzenesulfonamide
CAS No.:1333115-55-1
Molecular Formula:C₁₈H₁₅F₃N₂O₃S
Molecular Weight:396.39
Hs Code.:

Synonyms:(R,E)-N-(4-cyano-1-phenylbut-3-en-2-yl)-2-(trifluoromethoxy)benzenesulfonamide

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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 (R,E)-N-(4-cyano-1-phenylbut-3-en-2-yl)-2-(trifluoromethoxy)benzenesulfonamide

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Technology Process of (R,E)-N-(4-cyano-1-phenylbut-3-en-2-yl)-2-(trifluoromethoxy)benzenesulfonamide

There total 6 articles about (R,E)-N-(4-cyano-1-phenylbut-3-en-2-yl)-2-(trifluoromethoxy)benzenesulfonamide 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: 74.0%

: 1333115-54-0
(R,E)-4-amino-5-phenylpent-2-enenitrile

: 103008-51-1
2-(trifluoromethoxy)benzenesulfonyl chloride

: 1333115-55-1
(R,E)-N-(4-cyano-1-phenylbut-3-en-2-yl)-2-(trifluoromethoxy)benzenesulfonamide

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃; for 12h;

Reference yield:

: 19901-50-9,51987-73-6,77119-84-7
methyl (2R)-2-(t-butoxycarbonylamino)-3-phenylpropionate

: 1333115-55-1
(R,E)-N-(4-cyano-1-phenylbut-3-en-2-yl)-2-(trifluoromethoxy)benzenesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: diisobutylaluminium hydride / dichloromethane; toluene / 1 h / -78 °C / Inert atmosphere

1.2: 20 °C

2.1: 1,8-diazabicyclo[5.4.0]undec-7-ene; lithium chloride / acetonitrile / 1.5 h / 20 °C / Inert atmosphere

3.1: hydrogenchloride / methanol

4.1: triethylamine / dichloromethane / 12 h / 20 °C

With hydrogenchloride; diisobutylaluminium hydride; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; lithium chloride; In methanol; dichloromethane; toluene; acetonitrile;

Reference yield:

: 77119-85-8
N-(tert-butoxycarbonyl)-D-phenylalaninal

: 1333115-55-1
(R,E)-N-(4-cyano-1-phenylbut-3-en-2-yl)-2-(trifluoromethoxy)benzenesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1: 1,8-diazabicyclo[5.4.0]undec-7-ene; lithium chloride / acetonitrile / 1.5 h / 20 °C / Inert atmosphere

2: hydrogenchloride / methanol

3: triethylamine / dichloromethane / 12 h / 20 °C

With hydrogenchloride; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; lithium chloride; In methanol; dichloromethane; acetonitrile;