N-[1-(2,4-difluoro-3-phenoxy-phenyl)-propyl]-2-tritylsulfanyl-acetamide

Base Information

Chemical Name:N-[1-(2,4-difluoro-3-phenoxy-phenyl)-propyl]-2-tritylsulfanyl-acetamide
CAS No.:1434725-57-1
Molecular Formula:C₃₆H₃₁F₂NO₂S
Molecular Weight:579.71
Hs Code.:

Synonyms:N-[1-(2,4-difluoro-3-phenoxy-phenyl)-propyl]-2-tritylsulfanyl-acetamide

Suppliers and Price of N-[1-(2,4-difluoro-3-phenoxy-phenyl)-propyl]-2-tritylsulfanyl-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-[1-(2,4-difluoro-3-phenoxy-phenyl)-propyl]-2-tritylsulfanyl-acetamide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of N-[1-(2,4-difluoro-3-phenoxy-phenyl)-propyl]-2-tritylsulfanyl-acetamide

There total 11 articles about N-[1-(2,4-difluoro-3-phenoxy-phenyl)-propyl]-2-tritylsulfanyl-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:

: 1434720-26-9
(S)-1-(2,4-difluoro-3-phenoxy-phenyl)-propylamine

: 34914-36-8
2-(triphenylmethylthio)ethanoic acid

: 1434725-57-1
N-[1-(2,4-difluoro-3-phenoxy-phenyl)-propyl]-2-tritylsulfanyl-acetamide

Guidance literature:: With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 20 ℃; for 48h;

Reference yield:

: 261763-46-6
3-methyl-2,6-difluorophenol

: 1434725-57-1
N-[1-(2,4-difluoro-3-phenoxy-phenyl)-propyl]-2-tritylsulfanyl-acetamide

Guidance literature:: Multi-step reaction with 7 steps

1: cesium fluoride / acetonitrile / Inert atmosphere

2: N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile) / tetrachloromethane / 80 - 90 °C / Inert atmosphere

3: sodium hydrogencarbonate; dimethyl sulfoxide / 80 °C / Inert atmosphere

4: titanium(IV) tetraethanolate / dichloromethane / Inert atmosphere

5: tetrahydrofuran / 2 h / -78 °C / Inert atmosphere

6: hydrogenchloride / methanol; 1,4-dioxane / 1 h

7: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 48 h / 20 °C

With hydrogenchloride; titanium(IV) tetraethanolate; N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); sodium hydrogencarbonate; benzotriazol-1-ol; dimethyl sulfoxide; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; cesium fluoride; In tetrahydrofuran; 1,4-dioxane; methanol; tetrachloromethane; dichloromethane; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 98-80-6
phenylboronic acid

: 1434725-57-1
N-[1-(2,4-difluoro-3-phenoxy-phenyl)-propyl]-2-tritylsulfanyl-acetamide

Guidance literature:: Multi-step reaction with 5 steps

1: copper diacetate; pyridine; pyridine N-oxide / dichloromethane / 48 h / 20 °C / Molecular sieve

2: titanium(IV) tetraethanolate / dichloromethane / Inert atmosphere

3: tetrahydrofuran / 2 h / -78 °C / Inert atmosphere

4: hydrogenchloride / methanol; 1,4-dioxane / 1 h

5: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 48 h / 20 °C

With pyridine; pyridine N-oxide; hydrogenchloride; titanium(IV) tetraethanolate; copper diacetate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; N,N-dimethyl-formamide;