HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → 3-Ethyl-5-hexylsulfonamido-2-methylbenzoxazolium p-toluenesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Ethyl p-methylbenzenesulfonate | HCID 6638 | — |
| Reactant | 5-Hexylsulfonamido-2-methylbenzoxazole | HCID 15051064 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-Ethyl-5-hexylsulfonamido-2-methylbenzoxazolium p-toluenesulfonate | HCID 19993452 | — |
Reaction Conditions
| Temperature | 150 °C |
|---|
Reaction Steps
A mixture of 60 g of intermediate A and 44 g ethyl p-toluenesulfonate was heated in a round bottom flask at 150° C. for 5 minutes. Upon cooling to room temperature, the crude brown mass was almost solidified. The product was dissolved in 25 ml methanol and poured into 300 ml diethyl ether with rapid stirring for 1 hour. The solid precipitate was chilled at 2° C. overnight, and then filtered. The tan powder was thoroughly washed with ether and recrystallized from 200 ml hot isopropyl alcohol to yield 23.4 g of 3-ethyl-5-hexylsulfonamido-2-methylbenzoxazolium p-toluenesulfonate (Intermediate B).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04900653 |
| Source dataset | uspto-grants-1990_02 |
| ORD ID | ord-a0e387c961e1424b9d7c666584ccb238 |
| Source note | uspto-grants-1990_02 |