Reaktion #334361
ord-1bf2dee881c547ac8266ebe59e14e576
Reaktionsgleichung
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1Sonstigethe solution formed
- 2ExtraktionThe solution was extracted twice
- 3Sonstigeeach time with 30 ml of methyl tertiary butyl ether, the aqueous solution separated off
- 4Sonstigethe residual ether removed in a vacuum
- 5workup.ADDITIONThe solution was diluted with 200 ml of water, 7 mg of iron (III) sulfate
- 6workup.ADDITIONadded
- 7Filtrationthe precipitated iron salt filtered off
- 8Sonstigewas acidified with 10% hydrochloric acid at 5° C., to 10° C.
- 9workup.STIRRINGfurther stirred for 1 hour at pH 1
- 10Sonstigethe precipitated crude product
- 11Filtrationfiltered off
- 12WaschenThe precipitate was washed with water
- 13Sonstigedried in a vacuum
- 14Sonstigerecrystallized from ethyl acetate/hexane
- 15SonstigeAfter drying there
Vorschrift
8.0 grams (0.038 mole) of 6,8-dimercapto octanoic acid were added to 1.54 grams (0.038 mole) of sodium hydroxide in 90 ml of water and the solution formed adjusted to pH 9 with dilute aqueous sodium hydroxide. The solution was extracted twice, each time with 30 ml of methyl tertiary butyl ether, the aqueous solution separated off and the residual ether removed in a vacuum. The solution was diluted with 200 ml of water, 7 mg of iron (III) sulfate added and oxygen led in with stirring at room temperture. After 2.5 hours the reaction solution had reached a pH of 12.4, the supply of oxygen was ended and the precipitated iron salt filtered off. The clear yellow solution was acidified with 10% hydrochloric acid at 5° C., to 10° C., further stirred for 1 hour at pH 1 and the precipitated crude product filtered off. The precipitate was washed with water, dried in a vacuum and recrystallized from ethyl acetate/hexane. After drying there were obtained 5.9 grams (75% of theory) of 1,2-dithiolane-3-pentanoic acid as yellow crystals having a melting point of 61° C. to 62° C.