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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741590Generated: November 1, 2026

3-Fluorophenol → 2-Cyano-3-(3-fluorophenoxymethyl)pyridine

https://huagongshe.com/reaction/1741590

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-FluorophenolHCID 9743—
ReactantSodium ethoxideHCID 2723922—
ReactantSodiumHCID 5360545—
Reactant3-(Bromomethyl)pyridine-2-carbonitrileHCID 10375450—
SolventEthanolHCID 702—
Product2-Cyano-3-(3-fluorophenoxymethyl)pyridineHCID 10263162—

Reaction Steps

To a chilled solution of sodium ethoxide, prepared from 13.8 g of sodium metal and 240 ml of absolute ethanol, 56.9 ml of 3-fluorophenol was added and the mixture was stirred at room temperature for 30 minutes. Crude 3-bromomethyl-2-cyanopyridine (103 g) was added to the mixture at 5° C., and the mixture was reflexed for 2 hours. After being concentrated, the reaction mixture was diluted with ether, and the resultant insoluble materials were removed by filtration. The filtrate was washed with 10% aqueous sodium hydroxide solution and with water, dried over anhydrous sodium sulfate, and then concentrated. The residue was crystallized by trituration with a mixture of ether and n-hexane to yield 58.0 g of pale brown crystals, which were recrystallized from isopropyl ether to give pale yellow needles, mp 52°-53° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05334594
Source datasetuspto-grants-1994_08
ORD IDord-32e8dcd982d54917ba69b9a170485f54
Source noteuspto-grants-1994_08