Hydrochloric Acid → 2-(5-Methylpyridin-2-yl)ethan-1-amine
Reaktionsgleichung
[CH3:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][C:9]#[N:10])=[N:6][CH:7]=1.B.O1CCCC1.Cl.O>C1COCC1>[CH3:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][CH2:9][NH2:10])=[N:6][CH:7]=1Komponenten
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 60 °C
Versuchsvorschrift
To a solution of 18 g of crude 2-(5-methylpyridin-2-yl)acetonitrile in dry THF (100 mL) was added dropwise Borane-tetrahydrofuran complex (1.0 M in THF, 232 mL, 232.5 mmol, 4 eq) at 0° C. under N2 atmosphere. The reaction mixture was then heated to 60° C. overnight. The reaction was cooled to room temperature, aq. HCl (6 N, 40 mL) was added carefully and the reaction mixture was then heated at 70° C. for 2 hrs. After cooling, water was added and the resulting solution was washed with ether. The aqueous layer was basified with aq. NaOH (10 N) at 0° C. and saturated with K2CO3 then extracted with ether (5×100 mL). The organic layer was dried over MgSO4, filtered and evaporated to give 7.6 g of crude 2-(5-methylpyridin-2-yl)ethanamine. (96% crude yield)
Aufarbeitung
- temperatureThe reaction was cooled to room temperature
- temperaturethe reaction mixture was then heated at 70° C. for 2 hrs
- temperatureAfter cooling
- washthe resulting solution was washed with ether
- customwas basified with aq. NaOH (10 N) at 0° C. and saturated with K2CO3
- extractionthen extracted with ether (5×100 mL)
- dry with materialThe organic layer was dried over MgSO4
- filtrationfiltered
- customevaporated
Quellen und Nachweise
- ORD-Eintrag
- ord-e5fb3658f94146c8b2ad325633f9aa96
- Quelldatensatz
- uspto-grants-2012_04
- Patentnummer
- US08148536B2
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