Trifluoro-methanesulfonic acid 5-bromo-2-(4-methoxy-phenyl)-oxazol-4-yl ester

Base Information

Chemical Name:Trifluoro-methanesulfonic acid 5-bromo-2-(4-methoxy-phenyl)-oxazol-4-yl ester
CAS No.:178876-78-3
Molecular Formula:C₁₁H₇BrF₃NO₅S
Molecular Weight:402.145
Hs Code.:

Synonyms:Trifluoro-methanesulfonic acid 5-bromo-2-(4-methoxy-phenyl)-oxazol-4-yl ester

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Chemical Property of Trifluoro-methanesulfonic acid 5-bromo-2-(4-methoxy-phenyl)-oxazol-4-yl ester

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Technology Process of Trifluoro-methanesulfonic acid 5-bromo-2-(4-methoxy-phenyl)-oxazol-4-yl ester

There total 3 articles about Trifluoro-methanesulfonic acid 5-bromo-2-(4-methoxy-phenyl)-oxazol-4-yl ester 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: 45.0%

: 170235-12-8
2-(4-methoxyphenyl)-4-oxazolyl trifluoromethanesulfonate

: 178876-78-3
Trifluoro-methanesulfonic acid 5-bromo-2-(4-methoxy-phenyl)-oxazol-4-yl ester

Guidance literature:: With bromine; In benzene; for 1h; Ambient temperature;
DOI:10.1021/jo960433d

Reference yield:

: 3424-93-9
4-methoxyphenylacetamide

: 178876-78-3
Trifluoro-methanesulfonic acid 5-bromo-2-(4-methoxy-phenyl)-oxazol-4-yl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 2.) NaH / 1.) neat, 110 deg C, 2.) DME

2: 75 percent / 2,6-lutidine / CH₂Cl₂ / 5 h / Ambient temperature

3: 45 percent / Br₂ / benzene / 1 h / Ambient temperature

With 2,6-dimethylpyridine; bromine; sodium hydride; In dichloromethane; benzene;
DOI:10.1021/jo960433d

Reference yield:

: 57764-64-4
2-(4-methoxy-phenyl)-oxazol-4-one

: 178876-78-3
Trifluoro-methanesulfonic acid 5-bromo-2-(4-methoxy-phenyl)-oxazol-4-yl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 75 percent / 2,6-lutidine / CH₂Cl₂ / 5 h / Ambient temperature

2: 45 percent / Br₂ / benzene / 1 h / Ambient temperature

With 2,6-dimethylpyridine; bromine; In dichloromethane; benzene;
DOI:10.1021/jo960433d