Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 61924Generated: October 27, 2026

Oxalyl chloride → 2-[1-(2-Bromo-5-methoxyphenyl)cyclopropyl]benzofuran

https://huagongshe.com/reaction/61924

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant(2-Hydroxybenzyl)triphenylphosphonium bromideHCID 2724142—
ReactantHCID 66834787HCID 66834787—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product2-[1-(2-Bromo-5-methoxyphenyl)cyclopropyl]benzofuranHCID 6683440181.8%

Reaction Steps

To the DCM solution (6 ml) of 1-(2-bromo-5-methoxy-phenyl)-cyclopropane carboxylic acid (0.3 g, 1.1 mmol), DMF (2 drops) and oxalyl chloride (0.23 ml, 2.5 mmol) were added at room temperature, and the mixture was stirred at room temperature for 2 hrs. The residues obtained from the reaction solution after concentration under reduced pressure were dissolved in toluene (6 ml), added with (2-hydroxybenzyl)triphenylphosphonium bromide (0.605 g, 1.32 mmol) and TEA (0.46 ml, 3.3 mmol), and the resulting mixture was stirred and heated at 100° C. overnight. The residues obtained after concentration under reduced pressure were purified by silica gel column (hexane:DCM) to obtain the title compound (0.309 g, 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09440922B2
Source datasetuspto-grants-2016_09
ORD IDord-a3af345e73a24b86a904738f4e68d255
Source noteuspto-grants-2016_09