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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1023362Generated: November 1, 2026

2-Chlorobenzyl chloride → HCID 86673393, compound

https://huagongshe.com/reaction/1023362

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chlorobenzyl chlorideHCID 11906—
ReactantSodium hydrideHCID 24758—
ReactantHCID 67328977HCID 67328977—
SolventDimethylformamideHCID 6228—
ProductHCID 86673393HCID 86673393—

Reaction Steps

To a DMF (40 mL) solution of butyl (E)-3-{3-fluoro-4-[(5-hydroxypyridin-2-yl)oxy]phenyl}prop-2-enoate (3.82 g) and 2-chlorobenzyl chloride (1.6 mL) was added sodium hydride (60% w/w in oil, 0.60 g) at 0° C., and stirred at room temperature for 3 hours. The reaction mixture was quenched by addition of saturated NH4Cl (90 mL), and extracted with AcOEt. The organic layer was washed with water, saturated aqueous NaCl, dried over anhydrous Na2SO4, and evaporated. The residue was purified by silica gel column chromatography (n-hexane/AcOEt=19/1 to 9/1) to afford (E)-3-[4-({5-[(2-Chlorobenzyl)oxy]pyridin-2-yl}oxy)-3-fluorophenyl]prop-2-enoic acid butyl ester (3.53 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722663B2
Source datasetuspto-grants-2014_05
ORD IDord-c71b5f08e7934f708256a7d1e4ee0ab1
Source noteuspto-grants-2014_05