HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 9-(5-oxocyclopent-1-en-1-yl)nonanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | HCID 21767809 | HCID 21767809 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Ethyl 9-(5-oxocyclopent-1-en-1-yl)nonanoate | HCID 13046302 | — |
Reaction Steps
The acid ketone from Example 22 is Fisher esterfied with 100 ml. of absolute ethanol, 100 ml. of benzene, and 20 mg. of p-toluenesulfonic acid for 6 hours, cooled, and the solvent is evaporated. The resulting oil is dissolved in 3:1 benzene-ether and the solution is passed through a column of 100 g. of Florisil. The filtrate is evaporated and the residue is distilled to yield 2.97 g. of a colorless oil, b.p. 137°-139° C. (0.05 Torr).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | USRE029469 |
| Source dataset | uspto-grants-1977_11 |
| ORD ID | ord-1109b94c12b542baa0d528faee91f83d |
| Source note | uspto-grants-1977_11 |