HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclopentanone → HCID 67453590, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclopentanone | HCID 8452 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-(o-Tolyl)acetonitrile | HCID 31155 | — |
| Product | HCID 67453590 | HCID 67453590 | 11.7% |
Reaction Steps
The procedure outlined in example 1 is repeated with cyclopentanone (14.3 g, 0.17 mol), o-tolylacetonitrile (13.1 g, 0.10 mol) and KOH (1.12 g, 0.02 mol). Short path distillation of the crude at 0.05 mbar/124-130° C. yields 5.30 g (27% yield). The product is contaminated with α,α′-dicyclopentylidenecyclopentanone. It is further purified by FC on SiO2 to yield 2.3 g of oily product (10% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07655701B2 |
| Source dataset | uspto-grants-2010_02 |
| ORD ID | ord-209086fdb9274de09c6a963c18d4788b |
| Source note | uspto-grants-2010_02 |