N-[3-(2-bromoacetyl)-5-(pentafluorosulfanyl)phenyl]acetamide

Base Information

Chemical Name:N-[3-(2-bromoacetyl)-5-(pentafluorosulfanyl)phenyl]acetamide
CAS No.:1178584-06-9
Molecular Formula:C₁₀H₉BrF₅NO₂S
Molecular Weight:382.149
Hs Code.:

Synonyms:N-[3-(2-bromoacetyl)-5-(pentafluorosulfanyl)phenyl]acetamide

Suppliers and Price of N-[3-(2-bromoacetyl)-5-(pentafluorosulfanyl)phenyl]acetamide

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of N-[3-(2-bromoacetyl)-5-(pentafluorosulfanyl)phenyl]acetamide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of N-[3-(2-bromoacetyl)-5-(pentafluorosulfanyl)phenyl]acetamide

There total 9 articles about N-[3-(2-bromoacetyl)-5-(pentafluorosulfanyl)phenyl]acetamide 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:

: 1178585-41-5
N-[3-acetyl-5-(pentafluorosulfanyl)phenyl]acetamide

: 1178584-06-9
N-[3-(2-bromoacetyl)-5-(pentafluorosulfanyl)phenyl]acetamide

Guidance literature:: With phenyltrimethylammonium tribromide; In tetrahydrofuran; methanol; at 20 - 40 ℃; for 5h; Product distribution / selectivity; Inert atmosphere;

Reference yield:

: 1178585-39-1
N-methoxy-N-methyl-5-nitro-3-pentafluorosulfanylbenzamide

: 1178584-06-9
N-[3-(2-bromoacetyl)-5-(pentafluorosulfanyl)phenyl]acetamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: hydrogen / Raney nickel / methanol / 5 h / Inert atmosphere

2.1: triethylamine / dichloromethane / 3 h / 20 °C / Inert atmosphere

3.1: lithium hexamethyldisilazane / tert-butyl methyl ether; tetrahydrofuran / 0.5 h / 0 °C / Inert atmosphere

3.2: 5 h / 0 - 20 °C

3.3: Cooling with ice

4.1: phenyltrimethylammonium tribromide / tetrahydrofuran; methanol / 5 h / 20 - 40 °C / Inert atmosphere

With hydrogen; phenyltrimethylammonium tribromide; triethylamine; lithium hexamethyldisilazane; Raney nickel; In tetrahydrofuran; methanol; dichloromethane; tert-butyl methyl ether;

Reference yield:

: C₇H₃ClF₅NO₃S

: 1178584-06-9
N-[3-(2-bromoacetyl)-5-(pentafluorosulfanyl)phenyl]acetamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: N,N-diethyl-N-isopropylamine / dichloromethane / 1 h / 20 °C / Inert atmosphere

2.1: hydrogen / Raney nickel / methanol / 5 h / Inert atmosphere

3.1: triethylamine / dichloromethane / 3 h / 20 °C / Inert atmosphere

4.1: lithium hexamethyldisilazane / tert-butyl methyl ether; tetrahydrofuran / 0.5 h / 0 °C / Inert atmosphere

4.2: 5 h / 0 - 20 °C

4.3: Cooling with ice

5.1: phenyltrimethylammonium tribromide / tetrahydrofuran; methanol / 5 h / 20 - 40 °C / Inert atmosphere

With N,N-diethyl-N-isopropylamine; hydrogen; phenyltrimethylammonium tribromide; triethylamine; lithium hexamethyldisilazane; Raney nickel; In tetrahydrofuran; methanol; dichloromethane; tert-butyl methyl ether;