HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2191102Generated: October 30, 2026
Triphenylphosphine → HCID 72299154, compound
https://huagongshe.com/reaction/2191102
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Di-tert-butyl azodicarboxylate | HCID 97268 | — |
| Reactant | HCID 72299169 | HCID 72299169 | — |
| Reactant | 5-chloropyridin-2-ol | HCID 178516064 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 72299154 | HCID 72299154 | — |
Reaction Steps
In a 100 mL four necked round bottom flask with a magnetic stirrer and inert atmosphere 1.3 g polymer bound triphenylphosphine was stirred in 15 mL THF. At 0-5° C. a solution of 514 mg (2.23 mmol) di-tert-butyl azodicarboxylate in 8 mL THF and a solution of 271 mg (2.1 mmol) 5-chloro-2-hydroxypyridine in 10 mL THF was added. The mixture was stirred for 20 min at 0° C.-5° C. 441 mg (1.4 mmol) [(3RS, 4RS)-1-benzyl-3-(4-chloro-phenyl)-piperidin-4-yl]-methanol in 8 mL THF was added. The ice bath was removed and the brownish mixture was stirred for 2 h at room temperature. The mixture was filtrated over decalite and washed with ethyl acetate. The solvents were evaporated and the residue purified by column chromatography on silica gel eluting with ethyl acetate/toluene to yield after evaporation of the product containing fractions 0.3 g (50%) of the title compounds as white solid. MS (m/e): 298.3/427.1 [(M+H)+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08324248B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-7cdbf5a106704ed5ad603ff44dfed3fd |
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| Source note | uspto-grants-2012_12 |
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