HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → HCID 54500514, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Ethyl levulinate | HCID 10883 | — |
| Reactant | 3-Methylindole-1-ethanol | HCID 12226742 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 54500514 | HCID 54500514 | — |
Reaction Steps
A mixture of the intermediate of formula III, 3-methylindole-1-ethanol (29.7 g., 0.17 mole), described in Example 1, ethyl levulinate (26.96 g., 0.187 mole) and p-toluenesulfonic acid (2.25 g.) in dry benzene (650 ml.) is refluxed with stirring for 12 hr. with hydrated alkalialuminum silicate (Molecular Sieves #4). The benzene solution is washed with 5% aqueous NaHCO3, followed by water. Concentrations of the solution gave a residue, which is passed through a silica gel column using 15% ethyl acetate in benzene to afford the ester, 3,4-dihydro-1,10-dimethyl-1H-1,4-oxazino[4,3-a]indole-1-propionic acid ethyl ester, as an oil, γmaxCHCl3 1730 cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04066763 |
| Source dataset | uspto-grants-1978_01 |
| ORD ID | ord-d056ffb1104a478488c013df6dc05ffe |
| Source note | uspto-grants-1978_01 |