HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | (Triphenylphosphoranylidene)acetaldehyde | HCID 75051 | — |
| Reactant | 2-Quinolinecarboxaldehyde | HCID 79619 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Quinoline | HCID 7047 | — |
Reaction Steps
0.2 g (1.27 mmol) of 2-formylquinoline is dissolved in 10 ml of anhydrous toluene, in a dry round-bottomed flask equipped with a magnetic stirrer and a nitrogen inlet. 0.46 g (1.52 mmol) of (triphenylphosphoranylidene)acetaldehyde is added to this solution. The mixture is brought back to the reflux temperature of toluene for 90 minutes, and the solution is then slowly brought back to ambient temperature and hydrolyzed with 10 ml of water. After separation of the two phases, the aqueous phase is extracted with ethyl acetate (4×50 ml).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07342026B2 |
| Source dataset | uspto-grants-2008_03 |
| ORD ID | ord-e5faab79cb0d4274b7130ae8921c3bdc |
| Source note | uspto-grants-2008_03 |