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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334634Generated: October 30, 2026

Triphenylphosphine → 2-(5-Bromopent-1-ynyl)pyridine

https://huagongshe.com/reaction/334634

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantBromineHCID 24408—
Reactant5-(Pyridin-2-yl)pent-4-yn-1-olHCID 10997353—
SolventDichloromethaneHCID 6344—
Product2-(5-Bromopent-1-ynyl)pyridineHCID 6659792929%

Reaction Conditions

Temperature5 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883826B2
Source datasetuspto-grants-2014_11
ORD IDord-9313c62210014996a25cb65f7ca1bee0
Source noteuspto-grants-2014_11