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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 724247Generated: October 26, 2026

Acetonitrile → 2-Chloro-1-(3-fluoro-benzyloxy)-4-nitro-benzene

https://huagongshe.com/reaction/724247

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantPotassium CarbonateHCID 11430—
ReactantNitrofunginHCID 12074—
Reactant3-Fluorobenzyl bromideHCID 68007—
SolventWaterHCID 962—
Product2-Chloro-1-(3-fluoro-benzyloxy)-4-nitro-benzeneHCID 705926995.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

2-chloro-4-nitrophenol (9.02 g, 52 mmol)), 3-fluorobenzyl bromide (9.85 g, 52 mmol) and acetonitrile (90 mL) was combined at room temperature under nitrogen. Potassium carbonate (7.9 g, 57 mmol)) was added and the reaction mixture stirred at 60° C. for 2 hours and then cooled to room temperature. After cooling the reaction mixture was poured into water. The solids were collected by filtration and washed with diethyl ether to afford the desired product (13.98 g, 95% yield). [TLC system=1:1 EtOAc:Hexanes, Rf=0.76]

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07141576B2
Source datasetuspto-grants-2006_11
ORD IDord-3b9be54a4a434641b2bbbbcad2610482
Source noteuspto-grants-2006_11