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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1191003Generated: October 31, 2026

Acetic Acid → 4-(piperidin-1-ylmethyl)benzonitrile

https://huagongshe.com/reaction/1191003

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPiperidineHCID 8082—
Reactant4-CyanobenzaldehydeHCID 66042—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventMethanolHCID 887—
Product4-(piperidin-1-ylmethyl)benzonitrileHCID 753760354.1%

Reaction Steps

Under a nitrogen atmosphere, add sodium cyanoborohydride (5.77 g, 91.6 mmol) to a solution of 4-cyanobenzaldehyde (3 g, 22.9 mmol), piperidine (5.84 g, 68.7 mmol) and acetic acid (2.75 g, 45.8 mmol) in methanol (30 mL) at 0° C. with stirring. Warm the mixture to room temperature and stir overnight. Add water (100 mL), saturated aqueous K2CO3 (50 mL), and extract with DCM. Wash the combined organic extracts with water and brine. Dry the organic phase over Na2SO4, filter, and concentrate in vacuo. Purify by chromatography on silica gel (400 g) eluting with hexane/EtOAc (1:0 to 4:1 gradient) to obtain the desired intermediate as a clear oil (2.48 g, 54%). MS (APCI+) m/z: 201 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680091B2
Source datasetuspto-grants-2014_03
ORD IDord-67f9a992c6344b3bac0d680cfafb51b6
Source noteuspto-grants-2014_03