Sodium Sulfite → 6-Cyanohexane-l-sulfinic acid sodium salt

HRID 977646

Reaktionsgleichung

Reaktionsgleichung von HRID 977646
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]

Komponenten

5

Versuchsvorschrift

##STR13## In a three necked flask, fitted with a water condenser, a mechanical stirrer and a dropping funnel a solution of 1-bromo-6-cyanohexane (8.04 g, 42.3 mmol) was placed in 75 mL of 95% EtOH. 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 2h 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 collected by 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. 1H NMR (300 MHz, DMSO-d6) δ2.50 (t, j=8 Hz, 2H), 2.40(t, 8 Hz, 2H), 1.55 (m, 4H), 1.3(m, 4H).

Aufarbeitung

  1. temperatureThe mixture was heated
  2. temperatureto reflux and to it
  3. concentrationconcentrated under reduced pressure
  4. dissolutionThe residue was dissolved in 95% EtOH (200 ml)
  5. temperatureheated
  6. filtrationfiltered
  7. concentrationThe filtrate was concentrated
  8. temperaturecooled in an ice bath
  9. filtrationThe precipitate was collected by filtration
  10. customdried

Quellen und Nachweise

ORD-Eintrag
ord-2944157674b541c2adf9d044e2216ed9
Quelldatensatz
uspto-grants-1997_03
Patentnummer
US05614649

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