HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → 2,3-Dihydro-7-nitro-1-benzoxepin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | HCID 14580514 | HCID 14580514 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2,3-Dihydro-7-nitro-1-benzoxepin | HCID 14580515 | — |
Reaction Steps
300 ml of toluene are poured over 25.1 g (0.12 mole) of 5-hydroxy-7-nitro-2,3,4,5-tetrahydro-1-benzoxepin and, with the addition of 1.5 g of p-toluenesulfonic acid, the mixture is refluxed with a water trap for 2 hours. The cold reaction solution is washed with saturated sodium bicarbonate solution, water and saturated sodium chloride solution, dried over sodium sulfate and filtered, and the solvent is evaporated off in vacuo. The residue is a solid of melting point 94°-95.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05194442 |
| Source dataset | uspto-grants-1993_03 |
| ORD ID | ord-8d8a62111e8b48b684dea9c1090f4c05 |
| Source note | uspto-grants-1993_03 |