HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → N-Ethylphenothiazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Phenothiazine | HCID 7108 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Catalyst | Tetrabutylammonium hydrogen sulfate | HCID 94433 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-Ethylphenothiazine | HCID 219178 | — |
Reaction Steps
A mixture of 10 g (0.05 mol) of phenothiazine, 11.7 g (0.075 mol) of iodoethane, 4.2 g (0.075 mol) of potassium hydroxide and 0.25 g of tetra-n-butylammonium hydrogen sulfate in 200 ml of dry toluene was refluxed for 24 hours. After cooling, the reaction mixture was filtered, and the solvent was evaporated. The product was crystallized from methanol. The yield of 10-ethylphenothiazine (C14H13NS, FW=227.33) was 90%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07083884B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-625c6e1d30dd4d0a9f0e4279bcd0f5ff |
| Source note | uspto-grants-2006_08 |