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 | 78.7% |
Reaction Steps
In 24 ml of water and 24 ml of ethanol, 11.6 g of 2-amino-5-mercapto-1,3,4-thiadiazole and 3.8 g of sodium hydroxide were dissolved, 14.0 g of 1-bromohexane was added to this solution, and the mixture was heated to 70°-80° C. and stirred for 3 hours. After cooling, water was added and the mixture was filtered. The residue was washed with water, dried under reduced pressure, and recrystallized from an ethanol/n-hexane (1:1) mixture. Thus 14.5 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 | US04742063 |
| Source dataset | uspto-grants-1988_05 |
| ORD ID | ord-6432914c090d4f8787e299adb34c0060 |
| Source note | uspto-grants-1988_05 |