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

HRID 355341

Reaktionsgleichung

Reaktionsgleichung von HRID 355341
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 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 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) δ 2.50 (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. temperatureThe mixture was heated for 2 h
  4. concentrationconcentrated under reduced pressure
  5. dissolutionThe residue was dissolved in 95% EtOH (200 ml)
  6. temperatureheated
  7. filtrationfiltered
  8. concentrationThe filtrate was concentrated
  9. temperaturecooled in an ice bath
  10. filtrationThe precipitate was collected by filtration
  11. customdried

Quellen und Nachweise

ORD-Eintrag
ord-fcb052a2da6e477a924737dec9203cc3
Quelldatensatz
uspto-grants-1998_11
Patentnummer
US05830870

Verknüpfte Notizen

Wird geladen…