HuagongsheHuagongshe Chemistry Print Report · For research reference only
Morpholine → 4-[2-(Thiophen-2-yl)ethenyl]morpholine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | thienylethanal | HCID 6430722 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-[2-(Thiophen-2-yl)ethenyl]morpholine | HCID 54017439 | — |
Reaction Steps
A mixture of 1.5 g of 2-thienylacetaldehyde, 1.4 mL of morpholine, and 0.012 g of p-toluenesulfonic acid hydrate in 7.5 mL of toluene is heated at reflux under a Dean-Stark Trap with azeotropic removal of water for 3 hours. The solution is cooled, neutralized by the addition of solid sodium methoxide, and concentrated in vacuo. The residue is taken up in toluene, filtered, and concentrated in vacuo to afford the desired enamine as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05334576 |
| Source dataset | uspto-grants-1994_08 |
| ORD ID | ord-4656e1e58d284c8c94efb3e0cb10f85c |
| Source note | uspto-grants-1994_08 |