HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → 5,6-Dimethoxy-2-(4-pyridyl)methylene-1-indanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-Pyridinecarboxaldehyde | HCID 13389 | — |
| Reactant | 5,6-Dimethoxy-1-indanone | HCID 75018 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5,6-Dimethoxy-2-(4-pyridyl)methylene-1-indanone | HCID 53395132 | 90.2% |
Reaction Steps
A mixture of 5,6-dimethoxy-indan-1-one (10 g), pyridine-4-carboxaldehyde (7.8 g), p-toluenesulphonic acid (13.8 g) in toluene (120 ml) was refluxed azeotropically for 6 hours. The reaction mixture was cooled to room temperature and filtered. The wet solid so obtained was stirred with 10% aqueous sodium carbonate solution. The solid was filtered, washed with acetone and then dried to get the title compound (13.2 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08124783B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-2c94bbc0b36a4f348dcc56bbb273af71 |
| Source note | uspto-grants-2012_02 |