HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclopentanone → Benzene, 1-cyclopenten-1-yl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclopentanone | HCID 8452 | — |
| Reactant | 1-Phenyl-1-cyclopentanol | HCID 139165 | — |
| Product | Benzene, 1-cyclopenten-1-yl- | HCID 136652 | 90% |
Reaction Steps
The same experiment as in Example 2 was carried out, except for using 2.5 g (0.03 mol) cyclopentanone instead of 1.74 g of acetone. The resulting reaction mixture was analyzed by gas chromatography to confirm that the target 1-hydroxy-1-phenylcyclopentane and phenylcyclopentene were obtained in a yield of 90% in total.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07494962B2 |
| Source dataset | uspto-grants-2009_02 |
| ORD ID | ord-32ba6d161bff4e1c84a3bb5c159c951c |
| Source note | uspto-grants-2009_02 |