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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360116Generated: October 30, 2026

3-Pyridinecarboxaldehyde → Dipyridin-3-ylmethanol

https://huagongshe.com/reaction/1360116

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-PyridinecarboxaldehydeHCID 10371—
Reactant3-BromopyridineHCID 12286—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
ProductDipyridin-3-ylmethanolHCID 11309949—

Reaction Steps

n-BuLi (42 mL, 1.6M, 67 mmol) was added to a solution of 3-bromopyridine (5.9 mL, 9.74 g, 62 mmol) in ether (200 mL) at −78 C. The resulting yellow suspension was stirred for 1 h. A solution of nicotinaldehyde (5.3 mL, 6 g, 56 mmol) in ether (25 mL) was then added. After stirring for 0.5 h, the reaction mixture was allowed to warm gradually to 0 C. The reaction mixture was then quenched by addition of half saturated brine (100 mL). The resulting mixture was extracted once with ethyl acetate and once with chloroform. Drying (1:1 Na2SO4/K2CO3) and concentration gave dipyridin-3-ylmethanol as a very viscous orange oil which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879839B2
Source datasetuspto-grants-2011_02
ORD IDord-49143ba9d6ec48de8eef3d6b31c48539
Source noteuspto-grants-2011_02