Reacción #48463

Ecuación de reacción

Carbon disulfide

hydrochloric acid

2-Bromopropionamide

butanethiol

sodium hydroxide

→

title compound

2-amino-1-methyl-2-oxoethyl butyl trithiocarbonate

Disolventes

water

Acetone

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.STIRRINGthe solution was stirred for a further 20 min
2. 2
   workup.WAITthe mixture was left for 14 h
3. 3
   Otrothe volume was reduced to ca 100 mL by evaporation under reduced pressure
4. 4
   workup.ADDITIONThe residue was diluted with water (400 mL)
5. 5
   Extracciónextracted with ethyl acetate (400 mL)
6. 6
   LavadoThe organic layer was washed with water (100 mL) and saturated sodium chloride (100 mL)
7. 7
   Secadodried with sodium sulfate
8. 8
   Otroevaporated to dryness under reduced pressure
9. 9
   workup.DISSOLUTIONThe residue was dissolved in ether (200 mL)
10. 10
    workup.ADDITIONfilled with silica gel
11. 11
    ConcentraciónThe filtrate was concentrated to ca ½ volume

Procedimiento

Acetone (230 mL), tetrapropylammonium bromide (1.86 g, 6.67 mmol), and butanethiol (9.3 mL, 7.8 g, 8.8 mmol) were added to a solution of sodium hydroxide (3.5 g, 88 mmol) in water (12 mL), and the mixture was stirred in a stoppered flask for 20 min. Carbon disulfide (5.7 mL, 7.2 g, 95 mmol) was added and the solution was stirred for a further 20 min. 2-Bromopropionamide (13.3 g, 87.5 mmol) was added and the mixture was left for 14 h. The reaction was acidified with 2M hydrochloric acid (50 mL) and the volume was reduced to ca 100 mL by evaporation under reduced pressure. The residue was diluted with water (400 mL) and extracted with ethyl acetate (400 mL). The organic layer was washed with water (100 mL) and saturated sodium chloride (100 mL), dried with sodium sulfate and evaporated to dryness under reduced pressure. The residue was dissolved in ether (200 mL) and light petroleum (150 mL) and run through a 10 cm diameter Buchner funnel ¾ filled with silica gel. The filtrate was concentrated to ca ½ volume to give the title compound as a crop of yellow crystals (15.7 g, 76%). The silica gel was washed with ethyl acetate which was then combined with the mother liquors from the first crop of crystals. The resulting solution was evaporated to dryness under reduced pressure and partially purified by chromatography using ether/light petroleum. Recrystallisation from ether/light petroleum gave a second crop of the trithiocarbonate (3.76 g, 18%). An analytically pure sample was obtained by recrystallisation of the combined crops from ether/light petroleum (17.5 g, 84%).

Fuente