Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1810857Generated: October 25, 2026

Chlorosuccinimide → 2-Chloro-5-[2-(3-chloro-phenyl)-ethoxy]-4-methoxy-benzoic acid methyl ester

https://huagongshe.com/reaction/1810857

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
Reactantm-Chlorophenethylic alcoholHCID 78856—
ReactantMethyl 3-hydroxy-4-methoxybenzoateHCID 4056967—
Reactant3-[2-(3-Chloro-phenyl)-ethoxy]-4-methoxy-benzoic acid methyl esterHCID 67076296—
CatalystZirconium chloride (ZrCl4), (T-4)-HCID 9856075—
SolventDichloromethaneHCID 6344—
Product2-Chloro-5-[2-(3-chloro-phenyl)-ethoxy]-4-methoxy-benzoic acid methyl esterHCID 67076336—

Reaction Steps

Methyl 3-hydroxy-4-methoxybenzoate and 2-(3-chlorophenyl)-ethanol were reacted in analogy to step 1 of example 1. The obtained 3-[2-(3-chloro-phenyl)-ethoxy]-4-methoxy-benzoic acid methyl ester (300 mg, 0.935 mmol), N-chloro-succinimide (381 mg, 2.81 mmol), and zirconium tetrachloride (129 mg, 0.57 mmol) were suspended in DCM (4 ml) and the mixture was stirred under reflux for 5 h until the starting material was used up. The mixture was partitioned between EA and a saturated aqueous sodium hydrogencarbonate solution, the aqueous phase extracted with EA, and the combined organic extracts were dried over sodium sulfate, filtered and evaporated to dryness. The residue was purified by silica chromatography (HEP/EA gradient) to give 118 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362073B2
Source datasetuspto-grants-2013_01
ORD IDord-1f56a12b3a5f4d8d9d4bc253fdcd92dd
Source noteuspto-grants-2013_01