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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2275302Generated: October 30, 2026

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

https://huagongshe.com/reaction/2275302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant(2-Hydroxybenzyl)triphenylphosphonium bromideHCID 2724142—
Reactant1-(2-Bromo-5-methoxyphenyl)cyclopropane-1-carboxylic acidHCID 66834787—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product2-[1-(2-Bromo-5-methoxy-phenyl)-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 numberUS09126931B2
Source datasetuspto-grants-2015_09
ORD IDord-dea6a87af2e24481bcd47c382a250b06
Source noteuspto-grants-2015_09