Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1473540Generated: October 30, 2026

Acetic Acid → 2-Chloro-3'-fluoro-4-iodo-5-methoxy-1,1'-biphenyl

https://huagongshe.com/reaction/1473540

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSulfuric AcidHCID 1118—
ReactantN-IodosuccinimideHCID 120273—
Reactant2-Chloro-3'-fluoro-5-methoxy-1,1'-biphenylHCID 86687598—
SolventDichloromethaneHCID 6344—
Product2-Chloro-3'-fluoro-4-iodo-5-methoxy-1,1'-biphenylHCID 8668760085.1%

Reaction Steps

A round-bottom flask was charged with 2-chloro-3′-fluoro-5-methoxy-1,1′-biphenyl (1.288 g, 5.44 mmol), DCM (8.00 ml), AcOH (8.00 ml), and sulfuric acid (0.160 ml, 2.99 mmol) to give a clear solution. n-Iodosuccinimide (1.224 g, 5.44 mmol) was added in one portion to give a maroon-colored solution. After 7 h, the mixture was diluted with DCM, washed with water, washed with saturated aq. sodium thiosulfate, dried over sodium sulfate, filtered, and concentrated. The residue was purified by chromatography on silica gel (40-g Redi-Sep Gold column, 25-g silica gel column, 0-5% EtOAc/Heptane) give 2-chloro-3′-fluoro-4-iodo-5-methoxy-1,1′-biphenyl (1.68 g, 4.63 mmol, 85% yield) as a clear oil. m/z (ESI) 362.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012443B2
Source datasetuspto-grants-2015_04
ORD IDord-1cbd104094a04177ab5b95ed1858d325
Source noteuspto-grants-2015_04