HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromoethyl ethyl ether → HCID 178468143, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromoethyl ethyl ether | HCID 61141 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 178418936 | HCID 178418936 | — |
| Reactant | HCID 178527894 | HCID 178527894 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178468143 | HCID 178468143 | — |
Reaction Steps
The novel intermediate triazole compounds used in the above preparation were prepared as follows. To a solution of 11.8 g. sodium in 350 ml. absolute ethanol was added 52.5 g. 1,2,4-triazole-3-thiol. To the resulting solution was added 84 g. 1-bromo-2-ethoxyethane and the resulting solution refluxed for 3 hours. The cooled reaction mixture was filtered, the filtrate was evaporated under reduced pressure to remove solvent, and the residue was dissolved in ether. The resulting solution was filtered, the filtrate was evaporated to remove solvent and the residue distilled under reduced pressure to give 3-(2-ethoxyethylthio)-1,2,4-triazole, b.p. 337°-345° C./0.3-0.5 mm. Elemental analysis satisfactory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04251262 |
| Source dataset | uspto-grants-1981_02 |
| ORD ID | ord-500bb576e61a467d94839283c6c9b952 |
| Source note | uspto-grants-1981_02 |