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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1836995Generated: October 31, 2026

1,1-Dichloroethane → HCID 178526356, compound

https://huagongshe.com/reaction/1836995

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-DichloroethaneHCID 6365—
ReactantTriethylamineHCID 8471—
ReactantPhosphorus pentachlorideHCID 24819—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantHCID 12150613HCID 12150613—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductHCID 178526356HCID 17852635613%

Reaction Conditions

Temperature75 °C

Reaction Steps

To a dichloroethane solution of 7-pyrrolidin-1-yl-benzofuran-2-carboxylic acid (3-chloro-phenyl)-amide (343 mg, 1 μM) was added phosphorous pentachloride (210 mg, 1.2 mmol), and the mixture was stirred at 75° C. for 2 hours. The solvent was removed under vacuum, the mixture was treated with 5 ml of toluene and then was evaporated to dryness under vacuum. The residue was dissolved in acetonitrile and was added to another flask containing 210 mg (3 mmol) hydroxylamine hydrochloride and triethyl amine 701 μL (5 mmol) in acetonitrile at 0° C. The mixture was allowed to stir overnight. The reaction mixture was diluted with ethyl acetate, washed with 1 N HCl (2×) and brine. The organic layer was dried over MgSO4, filtered and stripped. The crude product was purified by flash chromatography on silica gel eluted with hexane/ethyl acetate (20:1) to give 43 mg of 3-chloro-N-(3-chloro-phenyl)-N′-hydroxy-7-pyrrolidin-1-yl-benzofuran-2-carboxamidine in 13% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06780858B2
Source datasetuspto-grants-2004_08
ORD IDord-104e81506e3e4debb7248071e92fab2a
Source noteuspto-grants-2004_08