2-amino-1-[2-(trifluoromethyl)phenyl]ethanol

Base Information

• Chemical Name: 2-amino-1-[2-(trifluoromethyl)phenyl]ethanol
• CAS No.: 133562-36-4
• Molecular Formula: C9H10F3NO
• Molecular Weight: 205.18
• Mol file: 133562-36-4.mol

Synonyms:2-amino-1-[2-(trifluoromethyl)phenyl]ethanol;AKOS BBV-002765;UKRORGSYN-BB BBV-002765

Chemical Property of 2-amino-1-[2-(trifluoromethyl)phenyl]ethanol

Chemical Property:

• Boiling Point: 292.6±35.0 °C(Predicted)
• PKA: 11.69±0.35(Predicted)
• PSA: 46.25000
• Density: 1.301±0.06 g/cm3(Predicted)
• LogP: 2.39780

Purity/Quality:

98%min ^*data from raw suppliers

2-amino-1-[2-(trifluoromethyl)phenyl]ethan-1-ol ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of 2-amino-1-[2-(trifluoromethyl)phenyl]ethanol

There total 4 articles about 2-amino-1-[2-(trifluoromethyl)phenyl]ethanol 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: 67.0%

2-nitro-1-(2-(trifluoromethyl)phenyl)ethan-1-ol → 2-hydroxy-2-[(2-trifluoromethyl)phenyl]ethanamine (133562-36-4)

Guidance literature:

With formic acid; hydrogen; In methanol; water;

DOI:10.1016/j.bmc.2017.05.055

Reference yield:

2-Trifluoromethylbenzaldehyde (447-61-0) → 2-hydroxy-2-[(2-trifluoromethyl)phenyl]ethanamine (133562-36-4)

Guidance literature:

Multi-step reaction with 2 steps

1: ZnI₂ / diethyl ether

2: LiAlH₄ / diethyl ether / Heating

With lithium aluminium tetrahydride; zinc(II) iodide; In diethyl ether;

DOI:10.1016/j.bmcl.2005.03.003

Reference yield:

2-(2-trifluoromethylphenyl)-2-trimethylsiloxyethanenitrile (82128-99-2) → 2-hydroxy-2-[(2-trifluoromethyl)phenyl]ethanamine (133562-36-4)

Guidance literature:

With lithium aluminium tetrahydride; In diethyl ether; Heating;

DOI:10.1016/j.bmcl.2005.03.003

upstream raw materials:

2-(2-trifluoromethylphenyl)-2-trimethylsiloxyethanenitrile

2-Trifluoromethylbenzaldehyde

Downstream raw materials:

2-({[3-(4-chlorophenyl)-5-oxo-4-(3,3,3-trifluoropropyl)-4,5-dihydro-1H-1,2,4-triazol-1-yl]acetyl}-amino)-1-[2-(trifluoromethyl)phenyl]ethyl carbamate

2-[({3-(4-chlorophenyl)-5-oxo-4-[(1E)-3,3,3-trifluoroprop-1-en-1-yl]-4,5-dihydro-1H-1,2,4-triazol-1-yl}acetyl)amino]-1-[2-(trifluoromethyl)phenyl]ethyl carbamate

2-({[3-(4-chlorophenyl)-4-(2-fluorobenzyl)-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl]acetyl}-amino)-1-[2-(trifluoromethyl)phenyl]ethyl carbamate

2-[({3-(4-chlorophenyl)-5-oxo-4-[(2S)-3,3,3-trifluoro-2-hydroxypropyl]-4,5-dihydro-1H-1,2,4-triazol-1-yl}acetyl)amino]-1-[2-(trifluoromethyl)phenyl]ethyl carbamate

Refernces

• 1、 -. "PYRIMDINE COMPOUNDS USEFUL AS KINASE INHIBITORS". Page/Page column 44. . Retrieved 2010/11/30.