(R)-1-[3,5-Bis(trifluoromethyl)phenyl]ethylamine HCl

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(R)-1-[3,5-Bis(trifluoromethyl)phenyl]ethylamine HCl Basic information
Product Name:(R)-1-[3,5-Bis(trifluoromethyl)phenyl]ethylamine HCl
Synonyms:(S)-1-[BIS-3,5-(TRIFLUOROMETHYL)PHENYL]ETHYLAMINE;(S)-ALPHA-METHYL-BIS-3,5-TRIFLUOROMETHYLBENZYLAMINE;S-MBT-PEM;(S)-1-(3,5-BIS(TRIFLUOROMETHYL)PHENYL)ETHANAMINE;(S)-1-[3,5-BIS(TRIFLUOROMETHYL)PHENYL]ETHYLAMINE;(1S)-1-[3,5-Bis(trifluoromethyl)phenyl]ethanamine;(R)-1-(3,5-Bis(trifluoromethyl)phenyl)ethanamine hydrochloride;Benzenemethanamine, α-methyl-3,5-bis(trifluoromethyl)-, (αS)-
CAS:127733-40-8
MF:C10H9F6N
MW:257.18
EINECS:
Product Categories:
Mol File:127733-40-8.mol
(R)-1-[3,5-Bis(trifluoromethyl)phenyl]ethylamine HCl Structure
(R)-1-[3,5-Bis(trifluoromethyl)phenyl]ethylamine HCl Chemical Properties
Boiling point 60/14mm
density 1.327±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka8.39±0.10(Predicted)
CAS DataBase Reference127733-40-8(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 22
Hazard Note Irritant
HS Code 2921490090
MSDS Information
(R)-1-[3,5-Bis(trifluoromethyl)phenyl]ethylamine HCl Usage And Synthesis
Uses(R)-1-(3,5-Bis(Trifluoromethyl)phenyl)ethanamine Hydrochloride is a useful reactant for the preparation of palladium complexes with chiral pincer ligands.
Synthesis
Benzenemethanamine, α-methyl-N-[(1S)-1-phenylethyl]-3,5-bis(trifluoromethyl)-, (αS)-

384824-41-3

Benzenemethanamine, α-methyl-N-[(1S)-1-phenylethyl]-3,5-bis(trifluoromethyl)-, (αR)-

511256-29-4

(R)-1-[3,5-BIS(TRIFLUOROMETHYL)PHENYL]ETHYLAMINE HCL

127733-40-8

(R)-1-[3,5-BIS(TRIFLUOROMETHYL)PHENYL]ETHYLAMINE

127733-47-5

The general procedure for the synthesis of (S)-1 -[3,5-bis(trifluoromethyl)phenyl]ethylamine and (R)-1 -[3,5-bis(trifluoromethyl)phenyl]ethylamine, using compound (CAS:384824-41-3) and compound (CAS:511256-29-4) as raw materials, is as follows: 181 mg (0.5 mmol) of the optically active crude product of secondary amine (4a) with 18 mg (0.25 wt%) of 5% palladium/activated carbon (water content: 50 wt%) was added to 2 mL of ethanol. Subsequently, the hydrogen pressure was set to 0.2 MPa and the reaction was stirred at 55°C for 12 hours. Upon completion of the reaction, the reaction solution was filtered through diatomaceous earth, the filtrate was concentrated and dried under vacuum to afford 96 mg of the crude product, i.e., optically active 1-(3,5-bis(trifluoromethyl)phenyl)ethylamine (5a), in 75% yield. The conversion was determined to be 99% by chiral gas chromatography (GC) analysis, the selectivity of the cleavage site (a:b) was 1:99, and the optical purity of the crude product was 76% ee.

References[1] Patent: US6797842, 2004, B2. Location in patent: Page column 19
Tag:(R)-1-[3,5-Bis(trifluoromethyl)phenyl]ethylamine HCl(127733-40-8) Related Product Information
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