HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl formate → 4-(Hydroxymethyl)piperidine-1-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl formate | HCID 7865 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Piperidinemethanol | HCID 420771 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(Hydroxymethyl)piperidine-1-carbaldehyde | HCID 22326884 | — |
Reaction Steps
4-Piperidinemethanol (10 g, 87 mmol) was dissolved in methyl formate (7 mL, 113 mmol) 0° C., and maintained at that temperature for 30 min, then allowed to reach 20° C. and stirred 90 min. Solid sodium hydroxide was added (0.87 g, pellets) and the mixture was left overnight. Dichloromethane was added, the NaOH removed by filtration and the solution treated with 1M HCl in ether (10 mL). The mixture was filtered through Celite and the solvent was removed under reduced pressure to afford the crude title compound. 1H NMR (400 MHz, CDCl3): 0.85-1.1 (2H, m); 1.55-1.85 (3H, m); 2.5-2.7 (1H, m); 2.95-3.1 (1H, m); 3.3 (2H, d, J 7 Hz); 3.6-3.7 (1H, m); 4.1-4.3 (1H, m); 8 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07442698B2 |
| Source dataset | uspto-grants-2008_10 |
| ORD ID | ord-cba3279ff78b4314b20e4220ed54aa47 |
| Source note | uspto-grants-2008_10 |