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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015622Generated: October 31, 2026

2,4-Dichlorobenzoyl chloride → HCID 67299348, compound

https://huagongshe.com/reaction/1015622

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 numberUS07985769B2
Source datasetuspto-grants-2011_07
ORD IDord-25d3093b2f104848a06c0d0f743997cf
Source noteuspto-grants-2011_07