HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2383382Generated: October 31, 2026
Potassium Carbonate → Benzyl 4-({3-[hydroxy(diphenyl)methyl]-1H-1,2,4-triazol-1-yl}methyl)piperidine-1-carboxylate
https://huagongshe.com/reaction/2383382
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Benzyl 4-(bromomethyl)piperidine-1-carboxylate | HCID 2776274 | — |
| Reactant | diphenyl(1H-1,2,4-triazol-5-yl)methanol | HCID 178519469 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Benzyl 4-({3-[hydroxy(diphenyl)methyl]-1H-1,2,4-triazol-1-yl}methyl)piperidine-1-carboxylate | HCID 59145967 | 81% |
Reaction Steps
Benzyl 4-(bromomethyl)piperidine-1-carboxylate (5 g, 16 mmol) was dissolved in dimethylformamide (40 ml) and diphenyl-(1H-[1,2,4]triazol-3-yl)-methanol (Tetrahedron: Asymmetry, 8(9), 1491-1500; 1997; 3.35 g, 13.65 mmol) added, followed by potassium carbonate (3.69 g, 26.7 mmol). After stirring at 70° C. for 18 hours the solvent was removed in vacuo, and the residue partitioned between ethyl acetate (150 ml) and water (150 mL). The organic layer was separated, dried over magnesium sulphate, filtered and the solvent removed in vacuo to furnish the title compound as a white solid in 81% yield, 5.2 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08263623B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-d621d1001885485288657c889dd2af88 |
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| Source note | uspto-grants-2012_09 |
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