Réaction #2267058
ord-35b097b0764b4dc9a89fcac955e74450
Équation de réaction
Réactifs
Solvants
Conditions de réaction
Traitement
- 1TempératureThe mixture was heated
- 2Températureto reflux
- 3Températureat reflux over night
- 4TempératureAs the mixture warmed the cream suspension
- 5workup.DISSOLUTIONgradually dissolved
- 6TempératureJust before refluxing
- 7Autreformed
- 8Filtrationfiltered
- 9Lavagethe residue was washed well with ethanol
- 10ConcentrationThe resulting filtrate was concentrated to dryness
- 11Autreto give an off-white solid
- 12Lavagewashed with 1) water (800 mL) and 2) brine (1 L)
- 13SéchageThe filtrate was dried (MgSO4)
- 14Concentrationconcentrated to dryness
- 15AutreAn off-white solid was obtained
- 16Autrethat was recrystallised
- 17LavageThe filtered material was washed well with acetonitrile
- 18Autredried (Vac/40° C.)
Mode opératoire
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%.