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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117631Generated: October 31, 2026

Methyl formate → 4-(Hydroxymethyl)piperidine-1-carbaldehyde

https://huagongshe.com/reaction/2117631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl formateHCID 7865—
ReactantSodium HydroxideHCID 14798—
Reactant4-PiperidinemethanolHCID 420771—
SolventDichloromethaneHCID 6344—
Product4-(Hydroxymethyl)piperidine-1-carbaldehydeHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442698B2
Source datasetuspto-grants-2008_10
ORD IDord-cba3279ff78b4314b20e4220ed54aa47
Source noteuspto-grants-2008_10