HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-(N-4-hydroxybutyl-N-butylamino)-4'-triflyl 1,4-diphenyl-1,3-butadiene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Triflylbenzyltriphenylphosphonium bromide | HCID 19795088 | — |
| Reactant | 4-(N-4-hydroxybutyl-N-butylamino)cinnamaldehyde | HCID 53997388 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-(N-4-hydroxybutyl-N-butylamino)-4'-triflyl 1,4-diphenyl-1,3-butadiene | HCID 86747243 | — |
Reaction Steps
To a stirred solution of 110 g (0.2 mole) of 4-triflylbenzyltriphenylphosphonium bromide in toluene is added dropwise 0.2 moles of n-BuLi at room temperature. After 2 hours a solution of 27.5 g (0.1 mole) of 4[N-4-hydroxybutyl-N-butylamino]cinnamaldehyde in toluene is added dropwise to the mixture, and the reaction is stirred for 18 hours at room temperature. Water is added, and compound C is isolated by vacuum filtration, washed with 60% ethanol/water, dried under vacuum, and purified by recrystallization from ethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05247042 |
| Source dataset | uspto-grants-1993_09 |
| ORD ID | ord-d48d928ccbcc4d238b26df05d712c5e6 |
| Source note | uspto-grants-1993_09 |