HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 1,5,6,7-Tetrahydro-4H-indol-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 4,5,6,7-Tetrahydro-1-benzofuran-4-one | HCID 2733541 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1,5,6,7-Tetrahydro-4H-indol-4-one | HCID 280229 | 96% |
Reaction Steps
To a mixture of 3 ml of ethanol and 7 ml of 29% aqueous ammonia was added 1.0 g of 4-oxo-4,5,6,7-tetrahydrobenzofuran, and then the mixture was subjected to reaction in a sealed tube at 150° C. for 12 hours. After completing the reaction, the reaction mixture was concentrated. The resulting residue was applied to a column of silica gel and eluted with a mixed solvent of acetone and ethyl acetate to give 950 mg (yield: 96%) of 4-oxo-4,5,6,7-tetrahydroindole being a light yellowish crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04558143 |
| Source dataset | uspto-grants-1985_12 |
| ORD ID | ord-6814b997cc814d20b1020941b9259c5c |
| Source note | uspto-grants-1985_12 |