HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1189162Generated: October 30, 2026
Triphenylphosphine → 2-(5-Bromopent-1-ynyl)pyridine
https://huagongshe.com/reaction/1189162
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 5-(Pyridin-2-yl)pent-4-yn-1-ol | HCID 10997353 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(5-Bromopent-1-ynyl)pyridine | HCID 66597929 | 29% |
Reaction Steps
Br2 (1.11 mL, 21.4 mmol) was added to a solution of triphenylphosphine (8.30 g, 30.7 mmol) in DCM (40 mL) at −5° C. A solution of 5-pyridin-2-yl-pent-4-yn-1-ol (3.00, 18.6 mmol) in DCM (10 mL) was added dropwise to the reaction mixture in order to maintain a temperature lower than 5° C. The reaction mixture was stirred for 5 hours at −10° C. and was quenched with a saturated solution of NaHCO3. The aqueous phase was extracted with DCM. The resulting organic phase was washed with brine, dried over MgSO4, filtered and evaporated. The crude residue was purified by flash chromatography (DCM/MeOH 99.5:0.5) to yield 2-(5-bromo-pent-1-ynyl)-pyridine (1.20 g, 5.35 mmol, 29%) with a purity of 50%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08674106B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-c915fc03a8e546f4957a9f424fd78674 |
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| Source note | uspto-grants-2014_03 |
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