HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3-dihydro-1H-indol-7-yl(phenyl)methanone → (1H-Indol-7-yl)(phenyl)methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3-dihydro-1H-indol-7-yl(phenyl)methanone | HCID 2741892 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (1H-Indol-7-yl)(phenyl)methanone | HCID 10878711 | — |
Reaction Steps
A reaction vessel is charged with 2.23 liters of methylene chloride to which is added one mole of the 7-benzoylindoline obtained in Example 1. To this mixture is added 3.0 moles of activated manganese dioxide. This reaction mixture is agitated and heated at reflux for 24 hours to produce 7-benzoylindole. The produce is then filtered through a filter that will retain the manganese dioxide. The reaction vessel is rinsed with 0.2 liter of hot methylene chloride and the filter cake washed with this rinse. The 7-benzoylindole product obtained has a melting point of 100°-104.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04221716 |
| Source dataset | uspto-grants-1980_09 |
| ORD ID | ord-39e855c8a0ec480799bc3e8abbf8c766 |
| Source note | uspto-grants-1980_09 |