HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Cyclopentanone, 2-(2-oxo-2-phenylethyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Phenacyl bromide | HCID 6259 | — |
| Reactant | Pyrrolidine, 1-(1-cyclopenten-1-yl)- | HCID 81570 | — |
| Product | Cyclopentanone, 2-(2-oxo-2-phenylethyl)- | HCID 10655725 | — |
Reaction Steps
A solution of 72.4 g (0.36 mole) of phenacyl bromide in 175 ml. of toluene is added dropwise to a stirred boiling solution of 50 g (0.036 mole) of 1-pyrrolidino-1-cyclopentene and 200 ml. of toluene. The reaction mixture is heated under reflux for 3 hours. diluted cautiously with 200 ml. of water, refluxed for 4 hours and cooled. After the layers separate, the aqueous phase is extracted with benzene, and the organic phase is dried and concentrated to an oil. Distillation gives 2-phenacylcyclopentanone as a liquid, b.p. 138°-140° C. (0.05 mm).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03997557 |
| Source dataset | uspto-grants-1976_12 |
| ORD ID | ord-e7e497e72e1e43f4901b79032a6ba84d |
| Source note | uspto-grants-1976_12 |