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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 245130Generated: October 25, 2026

4-Penten-1-OL → 2-Pyridinepentanol

https://huagongshe.com/reaction/245130

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Penten-1-OLHCID 13181—
Reactant9-Borabicyclo(3.3.1)nonaneHCID 78966—
Reactant4-Bromopyridinium chlorideHCID 88100—
SolventTetrahydrofuranHCID 8028—
SolventPotassium CarbonateHCID 11430—
SolventN,N-Dimethylformamide--water (1/1)HCID 21962138—
SolventHCID 178418397HCID 178418397—
Product2-PyridinepentanolHCID 1434747848%

Reaction Steps

9-Borabicyclo[3.3.1]nonane (9-BBN) dissolved in 15 ml of tetrahydrofuran (manufactured by Aldrich Co.) was added to 300 mg (3.483 mmol) of 4-pentene-1-ol and allowed to react at 25° C. for 24 hours. Then, 4-bromopyridine hydrochloride (manufactured by Aldrich Co.) dissolved in water/dimethylformamide (DMF) at a ratio of 2:8, tetrakis(triphenylphosphine)palladium (manufactured by Aldrich Co.), and potassium carbonate (manufactured by Aldrich Co.) were added thereto in an equivalent ratio of 1:1.2:0.2 and allowed to react at 70° C. for 6 hours. Then, solvent was removed under reduced pressure, and the residual material was diluted with ethyl acetate and filtered with Celite. The material thus obtained was purified by column chromatography (column: silica (manufactured by Aldrich Co.), solvent: ethyl acetate/hexane) to obtain 203 mg of pyridinepentanol (yield rate: 48%). The reaction scheme is shown below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658735B2
Source datasetuspto-grants-2014_02
ORD IDord-edf5fc161c754e968be6808e9781b3c9
Source noteuspto-grants-2014_02