HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → Ethyl {[5-(5-oxocyclopent-1-en-1-yl)pentyl]sulfanyl}acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | {[5-(5-Oxocyclopent-1-en-1-yl)pentyl]sulfanyl}acetic acid | HCID 20347252 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl {[5-(5-oxocyclopent-1-en-1-yl)pentyl]sulfanyl}acetate | HCID 20347243 | — |
Reaction Steps
A mixture of 74 g. (0.306 mols) of 2-(7-carboxy-6-thiaheptyl)-2-cyclopentenone, 1200 ml. of ethanol and 1 g. p-toluenesulfonic acid is stirred and refluxed for 18 hours. The resulting solution is concentrated and the residue is dissolved in ether. The organic phase is washed with water, sodium bicarbonate solution and saline, dried (MgSO4) and evaporated. The residue is distilled to give a light yellow oil, n.p. 147°-150° C. (0.07 Torr).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04194055 |
| Source dataset | uspto-grants-1980_03 |
| ORD ID | ord-b226376a5a9d406e803bc9f1590c473f |
| Source note | uspto-grants-1980_03 |