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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 219870Generated: October 25, 2026

2-Methylpiperidine → 5-Bromo-2-(2-methylpiperidin-1-YL)benzaldehyde

https://huagongshe.com/reaction/219870

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethylpiperidineHCID 7974—
ReactantSodium CarbonateHCID 10340—
Reactant5-Bromo-2-fluorobenzaldehydeHCID 736327—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product5-Bromo-2-(2-methylpiperidin-1-YL)benzaldehydeHCID 2309110189%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of 5-bromo-2-fluorobenzaldehyde (13.20 g; 65.02 mmol) in DMSO (160 mL) and water (40 mL) were added 2-methylpiperidine (15.35 mL; 130.04 mmol) and anhydrous sodium carbonate (13.78 g; 130.04 mmol). The resulting mixture was heated at 120° C. for 16 h after which it was allowed to cool to RT. Reaction mixture was partitioned between H2O (1 L) and Et2O (2×750 mL) and the combined organic layers were washed with brine (500 mL, pH 5-6 adjusted with HCl), dried over MgSO4, filtered and dried under vacuum to give the title compound as a brown yellow oil (16.3 g, 89%). LC/MS (Method B): 282.1 (M+H)+. HPLC (Method A): Rt 2.20 min (Purity: 93.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202865B2
Source datasetuspto-grants-2012_06
ORD IDord-98f3cacdfd4142f4b412f292328078fa
Source noteuspto-grants-2012_06