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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2093283Generated: November 1, 2026

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

https://huagongshe.com/reaction/2093283

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 numberUS08444988B2
Source datasetuspto-grants-2013_05
ORD IDord-01e0face01974130b62290932b8cbd2e
Source noteuspto-grants-2013_05