HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 4-(5H-Dibenzo(a,d)cyclohepten-5-ylidene)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 14119533 | HCID 14119533 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | 4-(5H-Dibenzo(a,d)cyclohepten-5-ylidene)piperidine | HCID 159718 | 102.5% |
Reaction Steps
A mixture of 65.6 g of ethyl 4-(5H-dibenzo[a,d]cyclohepten-5-ylidene)-1-piperidinecarboxylate, 32.0 g of potassium hydroxide and 250 ml of n-butanol was refluxed for 2 hrs and concentrated. Water was added to the residue and extracted with toluene. The toluene layer was washed with water, dried and concentrated to give 53.2 g of pale yellow solid, which was recrystallized from methanol to give 47.9 g of colorless needles, mp 145°-147° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05095022 |
| Source dataset | uspto-grants-1992_03 |
| ORD ID | ord-cd4d7f82458d4a32b7daf71d414bb0d7 |
| Source note | uspto-grants-1992_03 |