ChemicalBook--->CAS DataBase List--->22038-85-3

22038-85-3

22038-85-3 Structure

22038-85-3 Structure
IdentificationBack Directory
[Name]

(R)-2,2,2-TRIFLUORO-1-PHENYL-ETHYLAMINE
[CAS]

22038-85-3
[Synonyms]

Einecs 244-747-2
[(R)-α-(Trifluoromethyl)benzyl]amine
2,2,2-trifluoro-1-phenylethan-1-aMine
[R,(-)]-α-(Trifluoromethyl)benzylamine
(R)-2,2,2-TRIFLUORO-1-PHENYLETHANAMINE
(R)-(-)-α-(trifluoromethyl)benzylamine
(1R)-1-Phenyl-2,2,2-trifluoroethanamine
(1R)-2,2,2-trifluoro-1-phenylethanamine
(R)-2,2,2-TRIFLUORO-1-PHENYL-ETHYLAMINE
(R)-2,2,2-Trifluoro-1-phenylethan-1-amine
(R)-(-)-alpha-(trifluoromethyl)benzylamine
Benzenemethanamine, .alpha.-(trifluoromethyl)-, (.alpha.R)-
[EINECS(EC#)]

244-747-2
[Molecular Formula]

C8H8F3N
[MDL Number]

MFCD06738691
[MOL File]

22038-85-3.mol
[Molecular Weight]

175.15
Chemical PropertiesBack Directory
[Boiling point ]

196.4±40.0 °C(Predicted)
[density ]

1.224±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C(protect from light)
[pka]

6.15±0.10(Predicted)
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H319
[Precautionary statements ]

P264-P280-P305+P351+P338-P337+P313P
[Risk Statements ]

34
[Safety Statements ]

26-36/37/39
[RIDADR ]

3259
Spectrum DetailBack Directory
[Spectrum Detail]

(R)-2,2,2-TRIFLUORO-1-PHENYL-ETHYLAMINE(22038-85-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

2,2,2-TRIFLUORO-1-PHENYL-ETHYLAMINE

51586-24-4

(R)-2,2,2-TRIFLUORO-1-PHENYL-ETHYLAMINE

22038-85-3

General procedure for the synthesis of (R)-2,2,2-trifluoro-1-phenylethylamine from 1-phenyl-2,2,2-trifluoroethylamine: 1. Intermediate preparation: L-tartaric acid (36 g, 240.0 mmol) was added to a solution of 1-phenyl-2,2,2-trifluoroethylamine (40 g, 228.57 mmol) in isopropanol (400 mL). 2. Reaction: The reaction mixture was heated to reflux and maintained for 30 minutes. 3. Post-treatment: After completion of the reaction, the mixture was cooled to room temperature and the solid formed was collected by filtration. 4. Purification: The resulting solid was diluted with Na2CO3/H2O solution and subsequently extracted with dichloromethane (3 x 100 mL). 5. Drying and concentration: The organic phases were combined, dried over K2CO3 and subsequently concentrated under reduced pressure to afford the target product (1R)-2,2,2-trifluoro-1-phenylethylamine (12.5 g, 31% yield) as a white solid.

[References]

[1] Patent: WO2011/119701, 2011, A1. Location in patent: Page/Page column 40
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