HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde, 4-(diphenylamino)- → Benzenamine, 4-ethenyl-N,N-diphenyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde, 4-(diphenylamino)- | HCID 77846 | — |
| Reactant | HCID 22020909 | HCID 22020909 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Benzenamine, 4-ethenyl-N,N-diphenyl- | HCID 10869403 | — |
Reaction Steps
19 g of methylphosphonium bromide is suspended in dried THF under protective gas, and 6 g of potassium tert-butoxide are added in portions at 0° C. An immediate colour change to orange occurs. 14 g of N,N-diphenyl-p-aminobenzaldehyde are added to the reaction solution at 0° C. The mixture is warmed to room temperature and stirred for a further 20 hours. The solvent is stripped off in vacuo, the residue is taken up in dichloromethane, and the solution is extracted with water dried over magnesium sulfate, filtered, and the solvent is stripped off in vacuo.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09236571B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-9bd8aa99a9604f929763464e9696a24c |
| Source note | uspto-grants-2016_01 |