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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2245306Generated: October 30, 2026

Pyridine → (4-(2-Pyridyloxy)phenyl)methyl chloride

https://huagongshe.com/reaction/2245306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
Reactant[4-(Pyrid-2-yloxy)phenyl]methanolHCID 17859715—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product(4-(2-Pyridyloxy)phenyl)methyl chlorideHCID 22292927—

Reaction Conditions

Temperature22 °C

Reaction Steps

A stirred solution of 4.4 gram (0.037 mole) of thionyl chloride in 75 mL of dry methylene chloride was cooled to 0° C., and 0.07 gram (catalyst) of pyridine was added. A solution of 5.0 grams (0.025 mole) of (4-(2-pyridyloxy)phenyl)methanol in 25 mL of methylene chloride was then added drop wise. Upon completion addition of addition, the reaction mixture was allowed to warm to 22° C. where it stirred for 30 minutes. After this time an aliquot of the reaction mixture was taken up in ethyl acetate and treated with solid sodium bicarbonate. The organic layer was dried with sodium sulfate, filtered, and concentrated under reduced pressure to a residue. The NMR spectrum was consistent with the proposed structure. Inasmuch as this compound is unstable, it was used without further purification. The yield was estimated at about 5.0 grams.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07683070B2
Source datasetuspto-grants-2010_03
ORD IDord-5bda19a995a1434bb85d724f7ae1ecfd
Source noteuspto-grants-2010_03