| Identification | Back Directory | [Name]
N-methyl-N-(2,2,2-trifluoroethyl)amine hydrochloride | [CAS]
2730-52-1 | [Synonyms]
Methyl(2,2,2-trifluoroethyl)aMine, HCl 2,2,2-Trifluoro-N-MethylethanaMine HCl N-Methyl-N-(2,2,2-trifluoroethyl)aMine HCl 2,2,2-TRIFLUORO-N-METHYLETHANAMINIUM CHLORIDE N-Methyl-2,2,2-trifluoroethylamine Hydrochloride N-methyl-N-(2,2,2-trifluoroethyl)amine hydrochloride Ethanamine, 2,2,2-trifluoro-N-methyl-, hydrochloride (1:1) | [Molecular Formula]
C3H7ClF3N | [MDL Number]
MFCD08448126 | [MOL File]
2730-52-1.mol | [Molecular Weight]
149.54 |
| Chemical Properties | Back Directory | [Melting point ]
>200 °C (sublm)(Solv: ethanol (64-17-5)) | [storage temp. ]
Inert atmosphere,Room Temperature | [form ]
solid | [color ]
White | [InChI]
InChI=1S/C3H6F3N.ClH/c1-7-2-3(4,5)6;/h7H,2H2,1H3;1H | [InChIKey]
CUOWKFXFKFXJEL-UHFFFAOYSA-N | [SMILES]
C(CNC)(F)(F)F.[H]Cl |
| Hazard Information | Back Directory | [Synthesis]
General procedure for the synthesis of N-methyl-2,2,2-trifluoroacetamide hydrochloride from N-methyl-2,2,2-trifluoroacetamide: A solution was prepared by dissolving lithium aluminum hydride (69 g, 1.8 mol) in 100 mL of ether at 100 °C. To this solution, an ether solution of 2,2,2-trifluoro-N-methylacetamide (86 g, 0.6 mol) was slowly added at 0 °C. The reaction mixture was stirred at room temperature overnight. Subsequently, sodium sulfate decahydrate was added to the mixture at -10°C and the resulting suspension was filtered. Dry HCl gas was passed into the filtrate until a white solid precipitated. The solid product was separated by filtration and recrystallized with a solvent mixture of methanol/ether to give N-methyl-2,2,2-trifluoroethylamine hydrochloride as a final white solid (73 g, 80.7% yield). | [References]
[1] Patent: WO2010/131145, 2010, A1. Location in patent: Page/Page column 76 |
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SynAsst Chemical.
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021-60343070 |
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www.chemicalbook.com/ShowSupplierProductsList15848/0_EN.htm |
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