HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Aminophenol → HCID 21446102, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Aminophenol | HCID 403 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 13284199 | HCID 13284199 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 21446102 | HCID 21446102 | 82% |
Reaction Steps
92.8 g of 2-(2-oxo-cyclohexyl)-2-phenyl acetic acid and 44 g of 4-aminophenol in 800 cm3 of xylene were stirred and heated under reflux, as indicated in Example 1a), until the water formed in the reaction has been totally eliminated. This took 2 hours (volume collected: 14.2 cm3 ; theoretical: 14.4 cm3). After the distillation of 400 cm3 of solvent, the residue was cooled. The precipitate produced was collected and recrystallized from methylcellosolve to give 100 g (82%) of 1-(4-hydroxyphenyl)-2-oxo-3-phenyl-2,4,5,6,7,7a-hexahydro-indole (m.p. 241° C).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04015002 |
| Source dataset | uspto-grants-1977_03 |
| ORD ID | ord-e2a25d5670434c6792a5f11fb5df1fa6 |
| Source note | uspto-grants-1977_03 |