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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2350917Generated: November 2, 2026

Hydrochloric Acid → HCID 178420312, compound

https://huagongshe.com/reaction/2350917

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantSodium AzideHCID 33557—
Reactant4-Anilino-1-benzylpiperidine-4-carbonitrileHCID 70412—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178420312HCID 17842031247%

Reaction Steps

Sodium azide (5.85 g, 90 mmol) and 1-benzyl-4-cyano-4-anilinopiperidine (2.91 g, 10 mmol) were added slowly to a solution of AlCl3 (2.67 g, 20 mmole) in dry THF (100 ml). The resulting mixture was refluxed overnight. The reaction was quenched with water (50 ml). After separating the THF layer, the aqueous layer was extracted with additional THF (4×50 ml). The combined THF layers were dried over MgSO4 and concentrated in vacuo. The solid obtained was dissolved in 1N.HCl solution and the pH was adjusted to 6.0 with 1N NaOH solution. The resulting mixture was left overnight and filtered to give the product (1.58 g, 4.7 mmol) as white crystalline solid: mp 205°-206° C. (decomposed); IR (nujol) 3300 cm-1 ; NMR (270 MHz, DMSO-d6) δ2.2 to 2.7 (m, 8H, piperidine CH2), 3.53 (s, 2H, benzyl CH2), 6.35, 6.63 and 7.01 (3 m, 5H, anilinophenyl H's), 7.25 (m, 5H, benzylphenyl H's). Anal. Calcd. for C19H22N6 : C, 68.24; H, 6.63; N, 25.13. Found: C, 68.79; H, 6.76; N, 24.81. ##STR20##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04871749
Source datasetuspto-grants-1989_10
ORD IDord-ddda0ad1d3ec47e8bc08e1c50b79bf6f
Source noteuspto-grants-1989_10