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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1524023Generated: November 4, 2026

Acetonitrile → 6-((2-Bromophenoxy)methyl)picolinonitrile

https://huagongshe.com/reaction/1524023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
Reactant2-BromophenolHCID 7244—
ReactantCesium carbonateHCID 10796—
Reactant6-Chloromethyl-2-cyanopyridineHCID 10351875—
SolventEthyl AcetateHCID 8857—
Product6-((2-Bromophenoxy)methyl)picolinonitrileHCID 90313125—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a sealable 4 mL vial, containing 6-(chloromethyl)picolinonitrile (100 mg, 0.66 mmol) and 2-bromophenol (113 mg, 0.66 mmol), were added Cs2CO3 (320 mg, 0.98 mmol) and acetonitrile (1.7 mL). The vial was then heated at 80° Celsius for 15 hours. The reaction was then diluted with ethyl acetate, filtered through a celite plug and concentrated to dryness. The material was used without further purification. 1H NMR (500 MHz, CDCl3) δ 8.02-7.93 (m, 1H), 7.93-7.85 (m, 1H), 7.65-7.59 (dd, J=7.7, 1.1, 1H), 7.58-7.53 (dd, J=7.9, 1.6, 1H), 7.29-7.22 (m, 1H), 6.93-6.90 (dd, J=8.3, 1.3, 1H), 6.90-6.86 (m, 1H), 5.23 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09079866B2
Source datasetuspto-grants-2015_07
ORD IDord-a904456bc52d498689fc0cef7eb008ae
Source noteuspto-grants-2015_07