HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → HCID 12317491, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Catechol | HCID 289 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Ethyl 2-oxocyclopentanecarboxylate | HCID 69136 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 12317491 | HCID 12317491 | — |
Reaction Steps
A mixture of 15.7 g. of ethyl cyclopentanone-2-carboxylate, 11 g. of pyrocatechol, 0.5 g. of p-toluenesulphochloride and 0.5g. of p-toluenesulphonic acid in 100 cc. of anhydrous benzene is refluxed until the theoretical amount of water no longer distils azeotropically. The mixture is washed first with dilute NaOH and then with H2O until neutral. After drying with Na2SO4 the solvent is removed under vacuum. The residual oil is fractionated, and the desired product boils at 136°-139°C./0.3 mm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03969368 |
| Source dataset | uspto-grants-1976_07 |
| ORD ID | ord-7126e853b86140bcbd2b4e865e4ed389 |
| Source note | uspto-grants-1976_07 |