HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl p-methylbenzenesulfonate → HCID 23042805, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl p-methylbenzenesulfonate | HCID 6638 | — |
| Reactant | Iodide Ion | HCID 30165 | — |
| Reactant | HCID 23042801 | HCID 23042801 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 23042805 | HCID 23042805 | 121.4% |
Reaction Steps
Intermediate D (4.52 g) and ethyl p-toluenesulfonate (4.4 g) were combined in a large test tube and heated over a hot air gun with manual stirring for 5 minutes. A brownish melt formed, which solidified to a glass on cooling to room temperature. The glas was dissolved in 50 ml hot methanol, diluted with an 100 ml hot ethanol, and 9.0 g tetrabutylamonnium iodide dissolved in 20 ml ethanol was added. The brown, clear solution was cooled to room temperature and then ice cooled for 4 hours. Filtration of the resulting crystalline product gave 5.92 g of 3-ethyl-2-methyl-5-methylsulfonamidobenzoxazolium iodide (Intermediate E).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04940654 |
| Source dataset | uspto-grants-1990_07 |
| ORD ID | ord-02d98d6845c7439b9cc32c1ad5f1b3a9 |
| Source note | uspto-grants-1990_07 |