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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356127Generated: October 25, 2026

Dimethylformamide → 4-(Piperidin-1-yl)benzaldehyde

https://huagongshe.com/reaction/356127

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant1-PhenylpiperidineHCID 20038—
ReactantPhosphorus oxychlorideHCID 24813—
Solvent1,2-DichloroethaneHCID 11—
Product4-(Piperidin-1-yl)benzaldehydeHCID 29135440%

Reaction Steps

To a solution of 2.3 mL (30 mmoles) of N,N-dimethylformamide in 10 mL of 1,2-dichloroethane was added dropwise 2.8 mL (30 mmoles) of phosphorus oxychloride at 0° C. The ice-bath was removed and the reaction mixture was stirred for 15 min. 1-Phenylpiperidine (3.2 mL, 20 mmoles) was added to the above solution portionwise and the reaction mixture was refluxed overnight. The reaction mixture was poured into ice-cold 2N sodium hydroxide solution and stirred at room temperature for 1 h. The organic layer was separated and the aqueous layer was extracted with 2×20 mL of ethyl acetate. The combined organic layer was washed with brine until pH=7, dried over anhydrous sodium sulfate and evaporated. The residue was separated on a silica gel column eluting with ethyl acetate and hexane to afford 1.5 g (40%) of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05834504
Source datasetuspto-grants-1998_11
ORD IDord-3d3829a9d0bc4e199b4922eaac62b317
Source noteuspto-grants-1998_11