N-[2-(1-benzenesulfonyl-2-thiophen-2-yl-vinyl)-phenyl]-2,2,2-trifluoro-acetamide

Base Information

• Chemical Name: N-[2-(1-benzenesulfonyl-2-thiophen-2-yl-vinyl)-phenyl]-2,2,2-trifluoro-acetamide
• CAS No.: 869301-74-6
• Molecular Formula: C₂₀H₁₄F₃NO₃S₂
• Molecular Weight: 437.463
• Mol file: 869301-74-6.mol

Synonyms:N-[2-(1-benzenesulfonyl-2-thiophen-2-yl-vinyl)-phenyl]-2,2,2-trifluoro-acetamide

Chemical Property of N-[2-(1-benzenesulfonyl-2-thiophen-2-yl-vinyl)-phenyl]-2,2,2-trifluoro-acetamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of N-[2-(1-benzenesulfonyl-2-thiophen-2-yl-vinyl)-phenyl]-2,2,2-trifluoro-acetamide

There total 7 articles about N-[2-(1-benzenesulfonyl-2-thiophen-2-yl-vinyl)-phenyl]-2,2,2-trifluoro-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:

phosphoric acid 2-benzenesulfonyl-1-thiophen-2-yl-2-[2-(2,2,2-trifluoro-acetylamino)-phenyl]-ethyl ester diethyl ester → N-[2-(1-benzenesulfonyl-2-thiophen-2-yl-vinyl)-phenyl]-2,2,2-trifluoro-acetamide (869301-74-6)

Guidance literature:

With potassium tert-butylate; In tetrahydrofuran; at 0 ℃; for 1h;

DOI:10.1021/ol051826e

Reference yield:

N-(2-benzenesulfonylmethyl-phenyl)-2,2,2-trifluoro-acetamide (869301-68-8) → N-[2-(1-benzenesulfonyl-2-thiophen-2-yl-vinyl)-phenyl]-2,2,2-trifluoro-acetamide (869301-74-6)

Guidance literature:

Multi-step reaction with 3 steps

1.1: LHMDS / tetrahydrofuran / 0.5 h / -78 °C

1.2: tetrahydrofuran / 1 h / -78 °C

2.1: tetrahydrofuran / 2 h / 20 °C

3.1: 0.714 g / t-BuOK / tetrahydrofuran / 1 h / 0 °C

With potassium tert-butylate; lithium hexamethyldisilazane; In tetrahydrofuran;

DOI:10.1021/ol051826e

Reference yield:

N-[2-(1-benzenesulfonyl-2-hydroxy-2-thiophen-2-yl-ethyl)-phenyl]-2,2,2-trifluoro-acetamide → N-[2-(1-benzenesulfonyl-2-thiophen-2-yl-vinyl)-phenyl]-2,2,2-trifluoro-acetamide (869301-74-6)

Guidance literature:

Multi-step reaction with 2 steps

1: tetrahydrofuran / 2 h / 20 °C

2: 0.714 g / t-BuOK / tetrahydrofuran / 1 h / 0 °C

With potassium tert-butylate; In tetrahydrofuran;

DOI:10.1021/ol051826e

upstream raw materials:

N-(2-benzenesulfonylmethyl-phenyl)-2,2,2-trifluoro-acetamide

2-[(phenylsulfonyl)methyl]aniline

2-(phenylsulfonylmethyl)-1-nitrobenzene

sodium benzenesulfonate

Downstream raw materials:

2-(2-thienyl)indole