Sodium Carbonate → (R)-tetrahydrofuran-2-ylmethyl-cyanamide
Reaction equation
[N:1]#[C:2]Br.[C:4]([O-:7])([O-])=O.[Na+].[Na+].O1[CH2:14][CH2:13][CH2:12][C@@H:11]1[NH:15]C>CCOCC>[O:7]1[CH2:4][CH2:14][CH2:13][C@@H:12]1[CH2:11][NH:15][C:2]#[N:1]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a stirred mixture of cyanogen bromide (2.2 g, 20.8 mmol) and anhydrous Na2CO3 (4.2 g, 39.6 mmol) in dry ether (30 mL) cooled between −20 and −10° C. was added (R)-(tetrahydro-furan-2-yl)-methylamine (Aldrich) (2.0 g, 9.8 mmol) over 10 minutes. Stirring was continued for an additional 1.5 hours at −20 to −10° C. Then the mixture was filtered and concentrated to provide 2.21 g of the title product. MS (DCI/NH3) m/z 127 (M+H)+
Workup
- temperaturecooled between −20 and −10° C.
- filtrationThen the mixture was filtered
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-417d874678b54606bb4da77d683c8414
- Source dataset
- uspto-grants-2012_04
- Patent number
- US08158663B2
Reaction notes
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