methyl 2-(2-(3-trifluoromethylphenyl)-4-(1-(4-fluoro-N-methylphenylsulfonamido)ethyl)phenoxy)acetate

Base Information

Chemical Name:methyl 2-(2-(3-trifluoromethylphenyl)-4-(1-(4-fluoro-N-methylphenylsulfonamido)ethyl)phenoxy)acetate
CAS No.:1242846-66-7
Molecular Formula:C₂₅H₂₃F₄NO₅S
Molecular Weight:525.521
Hs Code.:

Synonyms:methyl 2-(2-(3-trifluoromethylphenyl)-4-(1-(4-fluoro-N-methylphenylsulfonamido)ethyl)phenoxy)acetate

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Chemical Property of methyl 2-(2-(3-trifluoromethylphenyl)-4-(1-(4-fluoro-N-methylphenylsulfonamido)ethyl)phenoxy)acetate

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Technology Process of methyl 2-(2-(3-trifluoromethylphenyl)-4-(1-(4-fluoro-N-methylphenylsulfonamido)ethyl)phenoxy)acetate

There total 5 articles about methyl 2-(2-(3-trifluoromethylphenyl)-4-(1-(4-fluoro-N-methylphenylsulfonamido)ethyl)phenoxy)acetate 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:

: 1242846-65-6
methyl 2-(2-(3-trifluoromethylphenyl)-4-(1-(methylamino)ethyl)phenoxy)acetate

: 349-88-2
4-Fluorobenzenesulfonyl chloride

: 1242846-66-7
methyl 2-(2-(3-trifluoromethylphenyl)-4-(1-(4-fluoro-N-methylphenylsulfonamido)ethyl)phenoxy)acetate

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; at 20 ℃; for 1h;

Reference yield:

: 99-93-4
4-Hydroxyacetophenone

: 1242846-66-7
methyl 2-(2-(3-trifluoromethylphenyl)-4-(1-(4-fluoro-N-methylphenylsulfonamido)ethyl)phenoxy)acetate

Guidance literature:: Multi-step reaction with 5 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: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 1 h / 20 °C

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

Reference yield:

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

: 1242846-66-7
methyl 2-(2-(3-trifluoromethylphenyl)-4-(1-(4-fluoro-N-methylphenylsulfonamido)ethyl)phenoxy)acetate

Guidance literature:: Multi-step reaction with 4 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: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 1 h / 20 °C

With sodium cyanoborohydride; potassium carbonate; N-ethyl-N,N-diisopropylamine; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; methanol; water; N,N-dimethyl-formamide; tert-butyl alcohol;