HuagongsheHuagongshe Chemistry Print Report · For research reference only
Salicylaldehyde → 2-(2-Morpholinoethoxy)benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Salicylaldehyde | HCID 6998 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Morpholine, 4-(2-chloroethyl)-, hydrochloride (1:1) | HCID 77210 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-(2-Morpholinoethoxy)benzaldehyde | HCID 976593 | — |
Reaction Steps
To a solution of salicylaldehyde (2 ml) in acetonitrile (20 ml) was added K2CO3 (5.71 g), followed by N-(2-chloroethyl)morpholine hydrochloride (3.5 g) and then the mixture was stirred at room temperature for 2 hours, then at reflux overnight. The reaction mixture was cooled to room temperature, filtered, and the filtrate was concentrated in vacuo to afford 2-[2-(4-morpholinyl)ethoxy]benzaldehyde, as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05958929 |
| Source dataset | uspto-grants-1999_09 |
| ORD ID | ord-5ea47cfc774c4e04a4b58b4e7e74100b |
| Source note | uspto-grants-1999_09 |