Reacción #334361
ord-1bf2dee881c547ac8266ebe59e14e576
Ecuación de reacción
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1Otrothe solution formed
- 2ExtracciónThe solution was extracted twice
- 3Otroeach time with 30 ml of methyl tertiary butyl ether, the aqueous solution separated off
- 4Otrothe residual ether removed in a vacuum
- 5workup.ADDITIONThe solution was diluted with 200 ml of water, 7 mg of iron (III) sulfate
- 6workup.ADDITIONadded
- 7Filtraciónthe precipitated iron salt filtered off
- 8Otrowas acidified with 10% hydrochloric acid at 5° C., to 10° C.
- 9workup.STIRRINGfurther stirred for 1 hour at pH 1
- 10Otrothe precipitated crude product
- 11Filtraciónfiltered off
- 12LavadoThe precipitate was washed with water
- 13Otrodried in a vacuum
- 14Otrorecrystallized from ethyl acetate/hexane
- 15OtroAfter drying there
Procedimiento
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.