HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414233Generated: October 29, 2026
Hydrochloric Acid → HCID 178420312, compound
https://huagongshe.com/reaction/414233
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | 4-Anilino-1-benzylpiperidine-4-carbonitrile | HCID 70412 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178420312 | HCID 178420312 | 47% |
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 (3m, 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. ##STR22##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04791120 |
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| Source dataset | uspto-grants-1988_12 |
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| ORD ID | ord-e8b285f006dd4887a884c363b4ce3d86 |
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| Source note | uspto-grants-1988_12 |
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