Reaction #2267058
ord-35b097b0764b4dc9a89fcac955e74450
Reaction equation
Reactants
Reagents
Solvents
Conditions
Workup
- 1TemperatureThe mixture was heated
- 2Temperatureto reflux
- 3Temperatureat reflux over night
- 4TemperatureAs the mixture warmed the cream suspension
- 5workup.DISSOLUTIONgradually dissolved
- 6TemperatureJust before refluxing
- 7Otherformed
- 8Filtrationfiltered
- 9Washthe residue was washed well with ethanol
- 10ConcentrationThe resulting filtrate was concentrated to dryness
- 11Otherto give an off-white solid
- 12Washwashed with 1) water (800 mL) and 2) brine (1 L)
- 13DryingThe filtrate was dried (MgSO4)
- 14Concentrationconcentrated to dryness
- 15OtherAn off-white solid was obtained
- 16Otherthat was recrystallised
- 17WashThe filtered material was washed well with acetonitrile
- 18Otherdried (Vac/40° C.)
Procedure
A three-necked 3-L round bottom flask was charged with 2-methylpentyl methanesulphonate (90 g, 0.5 mol), ethanol (1.5 L) and 2-mercapto-1,3,4-thiadiazole-5-amine (66.5 g, 0.5 mol). Sodium hydroxide (20 g, 0.5 mol) was added to the stirred suspension. The mixture was heated to reflux and held at reflux over night. As the mixture warmed the cream suspension gradually dissolved. Just before refluxing began a cloudy precipitate formed. The reaction mixture was cooled to room temperature, filtered, and the residue was washed well with ethanol. The resulting filtrate was concentrated to dryness to give an off-white solid that was dissolved in ethyl acetate (1.2 L) and washed with 1) water (800 mL) and 2) brine (1 L). The filtrate was dried (MgSO4) and concentrated to dryness. An off-white solid was obtained that was recrystallised from boiling acetonitrile (150 mL). The filtered material was washed well with acetonitrile and dried (Vac/40° C.). The required product was obtained as a white solid wt 83 g; 76.5%.