HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → 10-(1-Piperidinyl)-5H-dibenzo[a,d]cyclohepten-5-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 10-Bromo-5H-dibenzo[a,d][7]annulen-5-one | HCID 12437215 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 10-(1-Piperidinyl)-5H-dibenzo[a,d]cyclohepten-5-one | HCID 11098226 | — |
Reaction Steps
A mixture of 71.3 g of 10-bromo-5H-dibenzo[a,d]cyclohepten-5-one, 50 ml. of piperidine, 1 liter of t-butanol and finally 33.6 g of potassium t-butoxide was stirred under reflux 2 hours, then at room temperature overnight. The mixture was filtered, and concentrated to dryness. The residue was slurried with water and decanted. The residue was slurried with methanol and filtered to give 59.8 g of 10-(1-piperidyl)-5H-dibenzo[a,d]cyclohepten-5-one, m.p. 103°-105° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04399141 |
| Source dataset | uspto-grants-1983_08 |
| ORD ID | ord-0f26040b80254976847da16edf57f8f8 |
| Source note | uspto-grants-1983_08 |