HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222248Generated: October 26, 2026
Tetrahydrofuran → Tert-butyl 4-(5-phenyl-1,3,4-oxadiazol-2-yl)piperidine-1-carboxylate
https://huagongshe.com/reaction/222248
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | o-Toluenesulfonyl chloride | HCID 8623 | — |
| Reactant | HCID 40727882 | HCID 40727882 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | Tert-butyl 4-(5-phenyl-1,3,4-oxadiazol-2-yl)piperidine-1-carboxylate | HCID 21098365 | 99.8% |
Reaction Steps
To a mixture of tert-butyl 4-[(2-benzoylhydrazino)carbonyl]piperidine-1-carboxylate (3.00 g) and THF (60 mL) were added triethylamine (7.2 mL) and toluenesulfonyl chloride (4.94 g), followed by stirring at 50° C. overnight. The reaction liquid was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (hexane/ethyl acetate=95/5 to 80/20) to obtain tert-butyl 4-(5-phenyl-1,3,4-oxadiazol-2-yl)piperidine-1-carboxylate (2.84 g) as a colorless oily sub stance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08207199B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-583a514d5c4b4dd7af327b5a3d60ea85 |
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| Source note | uspto-grants-2012_06 |
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