HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → HCID 15333570, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 1-Naphthol | HCID 7005 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 9-Ethynyl-9-fluorenol | HCID 518771 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 15333570 | HCID 15333570 | — |
Reaction Steps
3.09 g of 9-ethynyl-9-fluorenol (15 mmoles) and 2.49 g of 1-naphthol (17.25 mmoles) were dissolved under reflux in 30 ml of anhydrous toluene in an inert atmosphere. 0.03 g of PTSA was then added. The reaction mixture was refluxed in an inert atmosphere for 2 hours 30 minutes. On returning to room temperature, the mixture was poured onto an aqueous 10% caustic soda solution. After decanting, the aqueous phase was continuously extracted with dichloromethane. The organic phases were combined and dried over magnesium sulphate. The solvent was removed under reduced pressure. The compound was precipitated out with hexane then recrystallised from toluene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05604280 |
| Source dataset | uspto-grants-1997_02 |
| ORD ID | ord-d7fe85af3ca54b73b2d76efcb984329f |
| Source note | uspto-grants-1997_02 |