| Identification | Back Directory | [Name]
tert-Butyl 2-(methylamino)ethylcarbamate | [CAS]
122734-32-1 | [Synonyms]
BUTTPARK 90\06-21
1-BOC-AMINO-2-METHYLAMINO-ETHANE
Boc-2-(Methylamino)ethylcarbamate
2-N-Boc-N1-methylethane-1,2-diamine
N-Boc-2-methylamino-ethylamine, 98%
1-Boc-Amino-2-methylamino-ethane ,98%
TERT-BUTYL 2-(METHYLAMINO)ETHYLCARBAMATE
1-BOC-Amino-2-methylamino-ethane(HClform)
tert-Butyl 2-(methylamino)ethylcarbamate HCl
tert-butyl N-[2-(MethylaMino)ethyl]carbaMate
N-(tert-Butoxycarbonyl)-N-methylethylenediamine
[2-(methylamino)ethyl]-, 1,1-dimethylethyl ester (9CI)
N-(tert-Butoxycarbonyl)-N'-methylethylenediamine≥ 98%(Titration)
N-(tert-Butoxycarbonyl)-N'-methylethylenediamine
Carbamic acid, [2-(methylamino)ethyl]-, 1,1-dimethylethyl ester (9CI) | [Molecular Formula]
C8H18N2O2 | [MDL Number]
MFCD06808585 | [MOL File]
122734-32-1.mol | [Molecular Weight]
174.24 |
| Chemical Properties | Back Directory | [Melting point ]
35 °C | [Boiling point ]
260.1±23.0 °C(Predicted) | [density ]
0.958±0.06 g/cm3(Predicted) | [storage temp. ]
Keep in dark place,Sealed in dry,Room Temperature | [solubility ]
soluble in Methanol | [form ]
powder to lump | [pka]
12?+-.0.46(Predicted) | [color ]
White to Almost white | [InChI]
InChI=1S/C8H18N2O2/c1-8(2,3)12-7(11)10-6-5-9-4/h9H,5-6H2,1-4H3,(H,10,11) | [InChIKey]
GKWGBMHXVRSFRT-UHFFFAOYSA-N | [SMILES]
C(OC(C)(C)C)(=O)NCCNC | [CAS DataBase Reference]
122734-32-1 |
| Hazard Information | Back Directory | [Chemical Properties]
White to very pale yellow solid | [Synthesis]
General procedure for the synthesis of tert-butyl 2-(methylamino)ethyl carbamate from (2-(benzyl(methyl)amino)ethyl)carbamate:
1. To a reaction flask were added 20% Pd(OH)2/carbon catalyst (3.1 g), tert-butyl (2-(benzyl(methyl)amino)ethyl)carbamate (3.3 g, 12.5 mmol), methanol (200 mL) and water (2 mL).
2. The reaction system was placed under a hydrogen atmosphere (40 psi) for 2.5 hours.
3. Upon completion of the reaction, the reaction mixture was filtered through diatomaceous earth and concentrated under vacuum to remove the solvent.
4. Water (50 mL) was added to the concentrate and the pH was adjusted to 12 with alkali.
5. The aqueous phase was extracted with dichloromethane (3 x 50 mL) and the organic layers were combined.
6. The organic layer was dried with anhydrous magnesium sulfate, filtered and concentrated in vacuum to give tert-butyl 2-(methylamino)ethylcarbamate (2.0 g, 11.7 mmol, 94% yield) as a colorless oil.
LC-MS [M + H] 686.5 (C35H51N5O7S + H, calculated value: 685.9). | [References]
[1] Patent: US2011/262355, 2011, A1. Location in patent: Page/Page column 136
[2] Patent: WO2011/133149, 2011, A1. Location in patent: Page/Page column 298
[3] Patent: WO2011/133150, 2011, A1. Location in patent: Page/Page column 300
[4] Patent: JP2016/41698, 2016, A. Location in patent: Paragraph 0364; 0377
[5] Patent: US2010/41748, 2010, A1. Location in patent: Page/Page column 120 |
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