Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206693Generated: October 25, 2026

Allyl bromide → 4-(Allyloxy)-5-bromo-2-chlorobenzonitrile

https://huagongshe.com/reaction/2206693

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Bromo-2-chloro-4-hydroxybenzonitrileHCID 53330452—
SolventAcetoneHCID 180—
Product4-(Allyloxy)-5-bromo-2-chlorobenzonitrileHCID 8671403665%

Reaction Steps

A mixture of compound 37 (20.5 g, 88.1 mmol), allyl bromide (11.2 mL, 132 mmol) and K2CO3 (24.4 g, 176 mmol) in acetone (440 mL) was stirred for 3 hours under reflux. The mixture was filtrated and concentrated in vacuo. The resultant was partitioned between EtOAc and water. The organic layer was washed with brine, dried over MgSO4, filtered and concentrated in vacuo. The residue was purified by silica gel column chromatography to afford the product 38 (15.6 g, 65%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371303B2
Source datasetuspto-grants-2016_06
ORD IDord-bdbbee18eaab4fd48597365336264816
Source noteuspto-grants-2016_06