HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromohexane → Sbb043676
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromohexane | HCID 8101 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 178509208 | HCID 178509208 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | Sbb043676 | HCID 1579472 | 77.1% |
Reaction Steps
In 190 ml of ethanol and 240 ml of water, 81.5 g of 2-amino-5-mercapto-1,3,4-thiadiazole and 26.9 g of sodium hydroxide were added. To this solution, 99 g of 1-bromohexane was added and the resulting mixture was warmed to 60°~70° C. and stirred for 2 hours. After cooling, water was added to the reaction mixture, and the resulting solution was filtered. The residue was washed with water and dried under reduced pressure. The dried residue was recrystallized from an ethanol/hexane mixture, and thus 100.5 g of 2-amino-5-hexylthio-1,3,4-thiadiazole was obtained. m.p. 113°~115° C. Yield 77%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04971971 |
| Source dataset | uspto-grants-1990_11 |
| ORD ID | ord-5267acc46329413ca55d2359d49b20ee |
| Source note | uspto-grants-1990_11 |