HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 555Generated: October 23, 2026
4-Bromopyridine → 1-(Pyridin-4-yl)pyrrolidin-3-ol
https://huagongshe.com/en/reaction/555
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Bromopyridine | HCID 14268 | — |
| Reactant | 4-Hydroxypyrrolidine | HCID 98210 | — |
| Reagent | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Catalyst | 2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenyl | HCID 2734217 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(Pyridin-4-yl)pyrrolidin-3-ol | HCID 21906198 | 43.01% |
Reaction Steps
In a 50 ml round bottomed flask THF (1 mL) was added to a mixture of 4-bromopyridine (1 g, 6.33 mmol), pyrrolidin-3-ol (0.662 g, 7.60 mmol),2-(dimethylamino)-2'-(dicyclohexylphosphino)biphenyl (0.249 g, 0.63 mmol) and Pd2(dba)3 (0.580 g, 0.63 mmol). To the slurry lithium bis(trimethylsilyl)amide (13.92 mL, 13.92 mmol) was added dropwise at 0 °C and the solution was refluxed at 65 °C overnight for 20 hrs. The reaction mixture was passed through celite, concentrated and column purified (0-20%MeOH/DCM) to obtain 0.447 mg of product.
Provenance & Evidence
| Source dataset | 750 AstraZeneca ELN dataset |
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| ORD ID | ord-15613520ef9b4d099659a0a3ac545228 |
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| Source note | 750 AstraZeneca ELN dataset |
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