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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1370818Generated: November 1, 2026

Allyl bromide → HCID 18512342, compound

https://huagongshe.com/reaction/1370818

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Fluoro-4-hydroxybenzonitrileHCID 2734675—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 18512342HCID 18512342—

Reaction Conditions

Temperature80 °C

Reaction Steps

2-Fluoro-4-hydroxybenzonitrile (5.00 g, 36.5 mmoles) and allyl bromide (3.47 mL, 40.1 mmoles) in anhydrous DMF (40 mL) were treated with K2CO3 (10.0 g, 72.9 mmoles) and stirred overnight at 80° C. Reaction mixture cooled and diluted with ethyl acetate, washed with H2O (2×) and brine, dried (Na2SO4), filtered, and concentrated under reduced pressure to provide the title compound with no further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06583180B2
Source datasetuspto-grants-2003_06
ORD IDord-c4a3c56e7fe5461db4ce22c2097dbd61
Source noteuspto-grants-2003_06