HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → 7-(2-thienyl)-1H-indene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 4-(2-Thienyl)-1-indanol | HCID 13102460 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 7-(2-thienyl)-1H-indene | HCID 13102462 | 96.3% |
Reaction Steps
A stirred solution of 2.4 g (0.011 mole) of 4-(2-thienyl)-1-indanol and 0.15 g of p-toluenesulfonic acid in 60 mL of toluene was heated under reflux, and the theoretical amount of water by-product was collected in a Dean-Stark trap. The reaction mixture was cooled and washed with two portions of 100 mL each of a 5% aqueous solution of sodium bicarbonate, then with two portions of 50 mL each of water. The organic layer was dried over magnesium sulfate, filtered, and the filtrate concentrated under reduced pressure to give 2.1 g of 7-(2-thienyl)-1H-indene as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04442296 |
| Source dataset | uspto-grants-1984_04 |
| ORD ID | ord-d76ef8475b984240bd37ee9b6fc1bd8f |
| Source note | uspto-grants-1984_04 |