N-[(E)-4-bromo-2-butenyl]-N-(tert-butyloxycarbonyl)[3-(perfluorooctyl)phenyl]sulfonamide

Base Information

Chemical Name:N-[(E)-4-bromo-2-butenyl]-N-(tert-butyloxycarbonyl)[3-(perfluorooctyl)phenyl]sulfonamide
CAS No.:335004-46-1
Molecular Formula:C₂₃H₁₉BrF₁₇NO₄S
Molecular Weight:808.351
Hs Code.:

Synonyms:N-[(E)-4-bromo-2-butenyl]-N-(tert-butyloxycarbonyl)[3-(perfluorooctyl)phenyl]sulfonamide

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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 N-[(E)-4-bromo-2-butenyl]-N-(tert-butyloxycarbonyl)[3-(perfluorooctyl)phenyl]sulfonamide

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Technology Process of N-[(E)-4-bromo-2-butenyl]-N-(tert-butyloxycarbonyl)[3-(perfluorooctyl)phenyl]sulfonamide

There total 4 articles about N-[(E)-4-bromo-2-butenyl]-N-(tert-butyloxycarbonyl)[3-(perfluorooctyl)phenyl]sulfonamide 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: 87.0%

: 821-06-7
(E)-1,4-dibromobutene

: 335004-16-5
N-(tert-butyloxycarbonyl)[3-(perfluorooctyl)phenyl]sulfonamide

: 335004-46-1
N-[(E)-4-bromo-2-butenyl]-N-(tert-butyloxycarbonyl)[3-(perfluorooctyl)phenyl]sulfonamide

Guidance literature:: With potassium carbonate; In acetonitrile; for 5h; Heating;
DOI:10.1002/1099-0690(200101)2001:2<329::aid-ejoc329>3.0.co;2-n

Reference yield:

: 87405-83-2
(heptadecafluorooctyl)benzene

: 335004-46-1
N-[(E)-4-bromo-2-butenyl]-N-(tert-butyloxycarbonyl)[3-(perfluorooctyl)phenyl]sulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1: chlorosulfonic acid / 120 °C

2: NH₃

3: 89 percent / Et₃N; DMAP / CH₂Cl₂

4: 87 percent / K₂CO₃ / acetonitrile / 5 h / Heating

With chlorosulfonic acid; dmap; ammonia; potassium carbonate; triethylamine; In dichloromethane; acetonitrile;
DOI:10.1002/1099-0690(200101)2001:2<329::aid-ejoc329>3.0.co;2-n

Reference yield:

: 104818-20-4
m-perfluoro-n-octylbenzenesulfonyl chloride

: 335004-46-1
N-[(E)-4-bromo-2-butenyl]-N-(tert-butyloxycarbonyl)[3-(perfluorooctyl)phenyl]sulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1: NH₃

2: 89 percent / Et₃N; DMAP / CH₂Cl₂

3: 87 percent / K₂CO₃ / acetonitrile / 5 h / Heating

With dmap; ammonia; potassium carbonate; triethylamine; In dichloromethane; acetonitrile;
DOI:10.1002/1099-0690(200101)2001:2<329::aid-ejoc329>3.0.co;2-n