2-((4-fluoro-3-(methylsulfonyl)phenyl)-4-((4-fluoro-N-methylphenylsulfonamido)methyl)phenoxy)acetic acid

Base Information

Chemical Name:2-((4-fluoro-3-(methylsulfonyl)phenyl)-4-((4-fluoro-N-methylphenylsulfonamido)methyl)phenoxy)acetic acid
CAS No.:1242844-96-7
Molecular Formula:C₂₃H₂₁F₂NO₇S₂
Molecular Weight:525.551
Hs Code.:

Synonyms:2-((4-fluoro-3-(methylsulfonyl)phenyl)-4-((4-fluoro-N-methylphenylsulfonamido)methyl)phenoxy)acetic acid

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Chemical Property of 2-((4-fluoro-3-(methylsulfonyl)phenyl)-4-((4-fluoro-N-methylphenylsulfonamido)methyl)phenoxy)acetic acid

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Technology Process of 2-((4-fluoro-3-(methylsulfonyl)phenyl)-4-((4-fluoro-N-methylphenylsulfonamido)methyl)phenoxy)acetic acid

There total 6 articles about 2-((4-fluoro-3-(methylsulfonyl)phenyl)-4-((4-fluoro-N-methylphenylsulfonamido)methyl)phenoxy)acetic acid 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: 73.0%

: 1242846-75-8
t-butyl 2-((4-fluoro-3-(methylsulfonyl)phenyl)-4-((4-fluoro-N-methylphenylsulfonamido)methyl)phenoxy)acetate

: 1242844-96-7
2-((4-fluoro-3-(methylsulfonyl)phenyl)-4-((4-fluoro-N-methylphenylsulfonamido)methyl)phenoxy)acetic acid

Guidance literature:: With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 2h;

Reference yield:

: 1836-06-2
3-bromo-4-hydroxyacetophenone

: 1242844-96-7
2-((4-fluoro-3-(methylsulfonyl)phenyl)-4-((4-fluoro-N-methylphenylsulfonamido)methyl)phenoxy)acetic acid

Guidance literature:: Multi-step reaction with 5 steps

1: potassium carbonate / N,N-dimethyl-formamide / 18 h / 20 °C

2: potassium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / water; tert-butyl alcohol / 0.33 h / 120 °C / microwave

3: sodium cyanoborohydride / methanol / 192 h / 20 °C

4: triethylamine / dichloromethane / 2.33 h / 0 - 20 °C

5: trifluoroacetic acid / dichloromethane / 8 h / 20 °C

With sodium cyanoborohydride; potassium carbonate; triethylamine; trifluoroacetic acid; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In methanol; dichloromethane; water; N,N-dimethyl-formamide; tert-butyl alcohol;

Reference yield:

: 99-93-4
4-Hydroxyacetophenone

: 1242844-96-7
2-((4-fluoro-3-(methylsulfonyl)phenyl)-4-((4-fluoro-N-methylphenylsulfonamido)methyl)phenoxy)acetic acid

Guidance literature:: Multi-step reaction with 6 steps

1: bromine / acetic acid / 0.5 h / 20 °C

2: potassium carbonate / N,N-dimethyl-formamide / 18 h / 20 °C

3: potassium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / water; tert-butyl alcohol / 0.33 h / 120 °C / microwave

4: sodium cyanoborohydride / methanol / 192 h / 20 °C

5: triethylamine / dichloromethane / 2.33 h / 0 - 20 °C

6: trifluoroacetic acid / dichloromethane / 8 h / 20 °C

With bromine; sodium cyanoborohydride; potassium carbonate; triethylamine; trifluoroacetic acid; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In methanol; dichloromethane; water; acetic acid; N,N-dimethyl-formamide; tert-butyl alcohol;