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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422358Generated: October 30, 2026

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

https://huagongshe.com/reaction/422358

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 numberUS08101637B2
Source datasetuspto-grants-2012_01
ORD IDord-e81b3580bbb3400388199bf16f58be3c
Source noteuspto-grants-2012_01