4-Fluoro-2-(2,2,2-trifluoroethoxy)aniline

Base Information

• Chemical Name: 4-Fluoro-2-(2,2,2-trifluoroethoxy)aniline
• CAS No.: 186386-90-3
• Molecular Formula: C₈H₇F₄NO
• Molecular Weight: 209.143
• Hs Code.: 2921420090
• European Community (EC) Number: 961-617-7
• Mol file: 186386-90-3.mol

Synonyms:4-FLUORO-2-(2,2,2-TRIFLUOROETHOXY)ANILINE;186386-90-3;SCHEMBL7821233;KTJBWMIVXDHCNT-UHFFFAOYSA-N;STL584291;AKOS000148071;MCULE-1413913503;CS-0261095;EN300-77084;G20915;A1-34793;Z240869726

Chemical Property of 4-Fluoro-2-(2,2,2-trifluoroethoxy)aniline

Chemical Property:

• XLogP3: 2.4
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 2
• Exact Mass: 209.04637650
• Heavy Atom Count: 14
• Complexity: 185

Purity/Quality:

99% ^*data from raw suppliers

4-fluoro-2-(2,2,2-trifluoroethoxy)aniline ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: C1=CC(=C(C=C1F)OCC(F)(F)F)N

Technology Process of 4-Fluoro-2-(2,2,2-trifluoroethoxy)aniline

There total 3 articles about 4-Fluoro-2-(2,2,2-trifluoroethoxy)aniline 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: 85.9%

4-fluoro-1-nitro-2-(2,2,2-trifluoroethoxy)benzene (186386-91-4) → 4-fluoro-2-(2,2,2-trifluoroethoxy)aniline (186386-90-3)

Guidance literature:

With iron; ammonium chloride; In ethanol; water; for 2.5h; Reflux;

Reference yield:

5-fluoro-2-nitrophenol (446-36-6) → 4-fluoro-2-(2,2,2-trifluoroethoxy)aniline (186386-90-3)

Guidance literature:

Multi-step reaction with 2 steps

1: 98 percent / Cs₂CO₃; NMP

2: Nickel boride; aq. HCl / methanol / 60 °C

With 1-methyl-pyrrolidin-2-one; hydrogenchloride; nickel boride; caesium carbonate; In methanol;

DOI:10.1016/S0960-894X(03)00305-6

Reference yield:

2,4-Difluoronitrobenzene (446-35-5) → 4-fluoro-2-(2,2,2-trifluoroethoxy)aniline (186386-90-3)

Guidance literature:

Multi-step reaction with 2 steps

1: caesium carbonate / tetrahydrofuran / 20 °C

2: ammonium chloride; iron / water; ethanol / 2.5 h / Reflux

With iron; ammonium chloride; caesium carbonate; In tetrahydrofuran; ethanol; water;

upstream raw materials:

4-fluoro-1-nitro-2-(2,2,2-trifluoroethoxy)benzene

5-fluoro-2-nitrophenol

2,4-Difluoronitrobenzene

Downstream raw materials:

3-(3-{4-[4-fluoro-2-(2,2,2-trifluoro-ethoxy)-phenyl]-piperazin-1-yl}-propyl)-5-hydroxymethyl-1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrimidine-2,4-dione

5-ethyl-3-(3-{4-[4-fluoro-2-(2,2,2-trifluoro-ethoxy)-phenyl]-piperazin-1-yl}-propyl)-1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrimidine-2,4-dione

3-(3-{4-[4-fluoro-2-(2,2,2-trifluoroethoxy)phenyl]piperazin-1-yl}propyl)-5-dimethylamino-1-[2-(trimethylsilyl)ethoxymethyl]-2,4(1H,3H)-pyrimidinedione

3-(3-{4-[4-fluoro-2-(2,2,2-trifluoro-ethoxy)-phenyl]-piperazin-1-yl}-propyl)-5-methoxy-1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrimidine-2,4-dione

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