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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1824480Generated: November 1, 2026

Piperidine → 2-(Piperidin-1-yl)benzaldehyde

https://huagongshe.com/reaction/1824480

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantPotassium CarbonateHCID 11430—
Reactanto-FluorobenzaldehydeHCID 67970—
SolventDimethylformamideHCID 6228—
Product2-(Piperidin-1-yl)benzaldehydeHCID 206215795.1%

Reaction Steps

A mixture of o-fluorobenzaldehyde (1.24 gm, 10 mmol), potassium carbonate (2.76 gm, 20 mmol), and piperidine (1.7 gm, 20 mmol) was refluxed in dry DMF for 6 hrs. After the completion of reaction DMF was distilled out at vaccum and 5 ml of water was added to the residue and extracted the product with ethyl acetate (10 ml×2). Organic layer was dried over sodium sulphate and evaporated the solvent to afford 1.8 gm of product (8) (90.5%) 1HNMR CDCl3 (Spectrum 9): 1.68(m, 6H), 3.05(m, 4H), 7.05(m, 2H), 7.45(dd, 1H), 7.75(dd, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07041830B2
Source datasetuspto-grants-2006_05
ORD IDord-528f4103d1a04abd80e280783f2ad730
Source noteuspto-grants-2006_05