Sodium Cyanide → HCID 21699526, compound
Reaction equation
[ClH:1].[NH:2]1[CH2:7][CH2:6]C[CH2:4][CH2:3]1.[CH2:8]([N:15]1[CH2:20][CH2:19][C:18](=O)[CH2:17][CH2:16]1)[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1.[C-]#N.[Na+]>CO.O.O>[ClH:1].[ClH:1].[C:9]1([C:8]2([N:15]3[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16]3)[CH2:6][CH2:7][NH:2][CH2:3][CH2:4]2)[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1Participants
6
Procedure
12.16 g of piperidine hydrochloride and 18.9 g of 1-benzylpiperid-4-one are dissolved in 50 ml of an MeOH/H2O mixture (50/50; v/v). 5.3 g of NaCN dissolved in 20 ml of water are added dropwise. After stirring for 48 hours, the precipitate formed is filtered, rinsed with water and dried to give 27 g of the expected product.
Workup
- additionare added dropwise
- customthe precipitate formed
- filtrationis filtered
- washrinsed with water
- customdried
Sources & evidence
- ORD record
- ord-b90e367f0dfe49cb9e9fd3e4daafb5a1
- Source dataset
- uspto-grants-2000_09
- Patent number
- US06124316
Reaction notes
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