Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196839Generated: October 29, 2026

1-Piperidinecarboxaldehyde → HCID 15017674, compound

https://huagongshe.com/reaction/1196839

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PiperidinecarboxaldehydeHCID 17429—
Reactant1-Bromo-2,4,5-trifluorobenzeneHCID 67597—
ReactantLithium diisopropylamideHCID 2724682—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15017674HCID 1501767445.3%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 1-bromo-2,4,5-trifluoro benzene (25 g, 0.12 mol) in THF (200 mL at -78° C. was added LDA (80 mL, 1.5 M) dropwise. The mixture was stirred at -78° C. for 1 hour, then N-formylpiperidine (16 g, 0.144 mol) was added in one portion and stirring continued for 2 hours. An additional 15 g of N-formylpiperidine was then added every 0.5 hour in 5 g portions. The reaction was quenched with 3N HCl (pH 3) at -78° C. The reaction was warmed to 0° C. and partitioned between H2O and ether. The ether layer was dried and concentrated and the residue was distilled to provide 13 g (45%) of the desired aldehyde; bp 63°-65° C. (0.2 mm).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05116834
Source datasetuspto-grants-1992_05
ORD IDord-84f19543d27e4a6f986004fbe8991e49
Source noteuspto-grants-1992_05