Reaction equation
Br[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][C:8]#[N:9].[S:10]([O-])([O-:12])=[O:11].[Na+:14].[Na+]>CCO.O>[Na+:14].[C:8]([CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2][S:10]([O-:12])=[O:11])#[N:9]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
In a three necked flask, fitted with a water condenser, a mechanical stirrer and a dropping funnel was placed a solution of 1-bromo-6-cyanohexane (8.04 g, 42.3 mmol) in 75 mL of 95% EtOH was prepared. The mixture was heated to reflux and to it was slowly added a solution of sodium sulfite (8.00 g, 63.5 mmol) in 50 mL of H2O over a period of 30 min. The mixture was heated for 2 h and then concentrated under reduced pressure. The residue was dissolved in 95% EtOH (200 ml), heated to boiling and filtered. The filtrate was concentrated and cooled in an ice bath. The precipitate was collectedby filtration and dried to give 3.00 g of a white solid. The mother liquor on further concentration, produced another batch of 2.2 g of the product.
Workup
- customIn a three necked flask, fitted with a water condenser, a mechanical stirrer and a dropping funnel
- customwas prepared
- temperatureThe mixture was heated
- temperatureto reflux and to it
- temperatureThe mixture was heated for 2 h
- concentrationconcentrated under reduced pressure
- dissolutionThe residue was dissolved in 95% EtOH (200 ml)
- temperatureheated
- filtrationfiltered
- concentrationThe filtrate was concentrated
- temperaturecooled in an ice bath
- filtrationfiltration
- customdried
Sources & evidence
- ORD record
- ord-dd6d62e26be04042bd06b5685fc85da9
- Source dataset
- uspto-grants-1996_08
- Patent number
- US05550262
Linked notes
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