Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propanal | HCID 527 | — |
| Reactant | Oxygen | HCID 977 | — |
| Reactant | Methylene blue cation | HCID 4139 | — |
| Reactant | Morpholine | HCID 8083 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Propanal | HCID 527 | — |
| Product | N-Formylmorpholine | HCID 20417 | — |
Reaction Steps
Mixture of propionaldehyde (VII, 2.73 mmole) and morpholine (5.76 mmole) in methylene chloride was irradiated for 90 min with oxygen bubbling in the presence of methylene blue. N-formylmorpholine was obtained in 103% yield on the basis of (VII), as expected. Further, mixture of propionaldehyde (2.73 mmole) and morpholine (11.52 mmole) gave N-formylmorpholine in 145% yield. When n-octylaldehyde (VIII) was used, the yield of N-formylmorpholine went up to 272% by irradiation for 240 min. (Table III.) Also the reaction of mixture of (VIII) and piperidine affords the same results. For example, N-formylpiperidine was obtained in 282% yield for 1.29 mmole of (VIII) and 20.5 mmole of (V). Also, N-formylpiperidine was obtained in 281% yield for the mole ratio of piperidine (V) to n-octylaldehyde (VIII) being 9 for 280 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04177121 |
|---|
| Source dataset | uspto-grants-1979_12 |
|---|
| ORD ID | ord-6cd1e9dbfd0946e4a7e83ef48f641e32 |
|---|
| Source note | uspto-grants-1979_12 |
|---|