HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methane → cis-2-(4-Hydroxy-phenyl)hexahydroisoindole-1,3-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methane | HCID 297 | — |
| Reactant | 4-Aminophenol | HCID 403 | — |
| Reactant | Hexahydrophthalic anhydride, cis- | HCID 641660 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | cis-2-(4-Hydroxy-phenyl)hexahydroisoindole-1,3-dione | HCID 7035660 | 69.5% |
Reaction Conditions
| Temperature | 170 °C |
|---|
Reaction Steps
A mixture of 4-aminophenol (5.46 g, 50.0 mmol) and cis-1,2-cyclohexanedicarboxylic anhydride (7.71 g, 50.0 mmol) was heated in a round bottom flask at 170° C. for 2 h. After cooling to room temperature the solid material was dissolved in hot ethanol (200 ml), activated charcoal was added and the solution was heated at reflux for 1 h. The solid material was removed by hot filtration. The solvent was partially evaporated. The solids were collected by filtration, washed quickly with a small amount of ethanol and dried in vacuo yielding the title compound (8.52 g, 69%, pink solid).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07067517B2 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-4faa3b6e1f554612b6bd92291aa0d0d5 |
| Source note | uspto-grants-2006_06 |