Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1800811Generated: November 2, 2026

Acetic Acid → 1-Methyl-4-phenylpiperidine-4-carbonitrile

https://huagongshe.com/reaction/1800811

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantFormaldehydeHCID 712—
Reactant4-Piperidinecarbonitrile, 4-phenyl-HCID 181138—
ReactantTriacetoxyborohydrideHCID 2724942—
SolventHydrochloric AcidHCID 313—
SolventDMF trimethylorthoformateHCID 86600666—
Product1-Methyl-4-phenylpiperidine-4-carbonitrileHCID 6251386.5%

Reaction Conditions

Temperature23 °C

Reaction Steps

4-Phenylpiperidine-4-carbonitrile (1.35 g, 6.062 mmol) was dissolved in N,N-dimethylformamide/trimethylorthoformate (1:1, 12 mL) and treated with paraformaldehyde (0.596 mL, 18.19 mmol), triacetoxyborohydride (3.854 g, 18.185 mmol) and acetic acid (1 mL). The mixture was stirred at 23° C. overnight, then diluted with 1N hydrochloric acid and washed with ethyl acetate. The aqueous phase was basified with aqueous sodium bicarbonate and extracted with ethyl acetate. The combined organic extracts were dried over anhydrous magnesium sulfate, filtered and concentrated to give the title material (1.05 g, 50%) as an oil. LC/MS (M+H)+: 200. HPLC ret. time (Condition B): 1.315 min. 1H NMR (400 MHz, CDCl3) δ ppm: 2.10-2.21 (4H, m), 2.41 (3H, s), 2.53 (2H, td, J=11.81, 3.41 Hz), 2.99 (2H, d, J=12.38 Hz), 7.32-7.38 (1H, m), 7.39-7.45 (2H, m), 7.49-7.54 (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08343999B2
Source datasetuspto-grants-2013_01
ORD IDord-98cf00fe16954366936ec96e30a0759e
Source noteuspto-grants-2013_01