HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanimidamide, N,N-diphenyl- → 2-(2-Anilinovinyl)-3-ethyl-5-hexylsulfonamidobenzoxazolium p-toluenesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanimidamide, N,N-diphenyl- | HCID 78296 | — |
| Reactant | 3-Ethyl-5-hexylsulfonamido-2-methylbenzoxazolium p-toluenesulfonate | HCID 19993452 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-(2-Anilinovinyl)-3-ethyl-5-hexylsulfonamidobenzoxazolium p-toluenesulfonate | HCID 86743744 | 87.8% |
Reaction Steps
A combination of 10 g Intermediate B and 8 g N,N-diphenylformamidine was thoroughly mixed and heated with stirring at 150°-160° C. for 25 minutes. The flask was then fitted with a condenser and 50 ml hot acetone was cautiously added. An orange precipitate formed. The flask was removed from the heat, cooled, and chilled in ice. After 1 hour, the reddish precipitate was filtered off and discarded. The filtrate was poured into 300 ml diethyl ether and stirred for 2 hors. The resulting yellow-orange powder was filtered, washed with ether, and dried to yield 10.6 g of 2-(2-anilinovinyl)-3-ethyl-5-hexylsulfonamidobenzoxazolium p-toluenesulfonate (Intermediate C).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04900652 |
| Source dataset | uspto-grants-1990_02 |
| ORD ID | ord-129ff1a456fc41a798c0e43b5d6a09b0 |
| Source note | uspto-grants-1990_02 |