(E)-2-(2-phenyl-2-(phenylimino)acetamido)phenyl trifluoromethanesulfonate

Base Information

Chemical Name:(E)-2-(2-phenyl-2-(phenylimino)acetamido)phenyl trifluoromethanesulfonate
CAS No.:1396629-85-8
Molecular Formula:C₂₁H₁₅F₃N₂O₄S
Molecular Weight:448.422
Hs Code.:

Synonyms:(E)-2-(2-phenyl-2-(phenylimino)acetamido)phenyl trifluoromethanesulfonate

Suppliers and Price of (E)-2-(2-phenyl-2-(phenylimino)acetamido)phenyl trifluoromethanesulfonate

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 (E)-2-(2-phenyl-2-(phenylimino)acetamido)phenyl trifluoromethanesulfonate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (E)-2-(2-phenyl-2-(phenylimino)acetamido)phenyl trifluoromethanesulfonate

There total 4 articles about (E)-2-(2-phenyl-2-(phenylimino)acetamido)phenyl trifluoromethanesulfonate 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: 78.0%

: 1334682-12-0
trifluoromethanesulfonic acid 2-(2-oxo-2-phenylacetylamido)phenyl ester

: 62-53-3
aniline

: 1396629-85-8
(E)-2-(2-phenyl-2-(phenylimino)acetamido)phenyl trifluoromethanesulfonate

Guidance literature:: With sodium hydrogencarbonate; In toluene; at 80 ℃; for 24h; Molecular sieve; Inert atmosphere; Sealed tube;
DOI:10.1021/ol302119j DOI:10.1021/ol302119j

Reference yield:

: 1334683-40-7
C₁₄H₁₁NO₃

: 1396629-85-8
(E)-2-(2-phenyl-2-(phenylimino)acetamido)phenyl trifluoromethanesulfonate

Guidance literature:: Multi-step reaction with 2 steps

1: pyridine / dichloromethane / 2 h / 0 - 20 °C / Inert atmosphere

2: sodium hydrogencarbonate / toluene / 24 h / 80 °C / Molecular sieve; Inert atmosphere; Sealed tube

With pyridine; sodium hydrogencarbonate; In dichloromethane; toluene;
DOI:10.1021/ol302119j DOI:10.1021/ol302119j

Reference yield:

: 611-73-4
Benzoylformic acid

: 1396629-85-8
(E)-2-(2-phenyl-2-(phenylimino)acetamido)phenyl trifluoromethanesulfonate

Guidance literature:: Multi-step reaction with 4 steps

1: oxalyl dichloride; N,N-dimethyl-formamide / dichloromethane / 0 - 20 °C / Inert atmosphere

2: triethylamine / dichloromethane / 0 - 20 °C / Inert atmosphere

3: pyridine / dichloromethane / 2 h / 0 - 20 °C / Inert atmosphere

4: sodium hydrogencarbonate / toluene / 24 h / 80 °C / Molecular sieve; Inert atmosphere; Sealed tube

With pyridine; oxalyl dichloride; sodium hydrogencarbonate; triethylamine; N,N-dimethyl-formamide; In dichloromethane; toluene;
DOI:10.1021/ol302119j DOI:10.1021/ol302119j