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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2193906Generated: November 1, 2026

2,4-Dichlorobenzoyl chloride → HCID 67299348, compound

https://huagongshe.com/reaction/2193906

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Dichlorobenzoyl chlorideHCID 66645—
ReactantHCID 20775770HCID 20775770—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
ProductHCID 67299348HCID 6729934878%

Reaction Steps

To a stirred solution of 5-Phenyl-3-{[5-(3-trifluoromethyl-phenyl)-furan-2-ylmethyl]-amino}-thiophene-2-carboxylic acid methylester (65 mg 0.142 mmol) in dichloromethane (3 ml) and saturated NaHCO3 solution (3 ml) was added a solution of 2,4-dichloro-benzoyl chloride (36 mg, 1.2 eq.) in dichloromethane (0.9 ml). The reaction mixture was stirred vigorously at room temperature for overnight. The organic phase was collected and the aqueous phase was extracted twice with methylene chloride (2×15 ml). The organic layers were combined, washed with water, brine and dried over anhydrous Na2SO4. Solvent was removed and residue was purified on silica gel using Hexane:EtOAc 9:1 as eluant to give the desired product in 78% yield (70 mg). The proton NMR indicated the presence of rotamers.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329924B2
Source datasetuspto-grants-2012_12
ORD IDord-8dbbd8d1e2964dd99266bf7851036d93
Source noteuspto-grants-2012_12