HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → 2H-Pyran, tetrahydro-2-(4-iodophenoxy)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| Reactant | 4-Iodophenol | HCID 10894 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2H-Pyran, tetrahydro-2-(4-iodophenoxy)- | HCID 2916803 | — |
Reaction Steps
10 Grams of p-iodophenol, 8 ml of dihydropyrane and a catalytic amount of p-toluenesulfonic acid was dissolved in 30 ml of anhydrous diethyl ether, and the mixture was stirred at room temperature for 2 hours. The reaction mixture was washed with water, dried then the solvent was removed by evaporation to yield 12.4 g of 4-(2-tetrahydropyranyloxy)-1-iodobenzene in the form of yellow oily substance. Boiling point: 84°-87° C. (at 25 mm Hg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04795814 |
| Source dataset | uspto-grants-1989_01 |
| ORD ID | ord-a14ba10efab34592a258f36ac5975bb4 |
| Source note | uspto-grants-1989_01 |