Methylamine → 1269615-30-6
Reaktionsgleichung
Cl[CH2:2][C:3]1[N:4]=[N:5][N:6]([CH3:8])[N:7]=1.[CH3:9][NH2:10]>>[CH3:9][NH:10][CH2:2][C:3]1[N:4]=[N:5][N:6]([CH3:8])[N:7]=1Komponenten
3
Reaktionsbedingungen
- Temperatur
- 45 °C
Versuchsvorschrift
To 5-(chloromethyl)-2-methyl-2H-tetrazole (136.8 mg, 1.032 mmol), was added methylamine (4.00 mL of 2M solution in THF, 8.00 mmol). This was stirred for 16 hours at 45° C. A white precipitate formed in the reaction and it was allowed to continue stirring for another 24 hours at room temperature before being concentrated in vacuo and successively azeotroped with THF, triethylamine, methanol, and then DCM. 1H NMR (600 MHz, CDCl3) δ 2.23 (s, 3H), 3.80 (s, 2H), 4.29 (s, 3H).
Aufarbeitung
- customA white precipitate formed in the reaction and it
- stirringto continue stirring for another 24 hours at room temperature
- concentrationbefore being concentrated in vacuo
- customsuccessively azeotroped with THF, triethylamine, methanol
Quellen und Nachweise
- ORD-Eintrag
- ord-0bcd22bebf4d40928a69a85fd30ac9f7
- Quelldatensatz
- uspto-grants-2013_12
- Patentnummer
- US08604038B2
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