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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2186016Generated: October 30, 2026

Benzoyl chloride → HCID 53746038, compound

https://huagongshe.com/reaction/2186016

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantHCID 15907988HCID 15907988—
SolventPyridineHCID 1049—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 53746038HCID 53746038—

Reaction Conditions

Temperature0 °C

Reaction Steps

To an ice cooled solution of N-(4-{3-[3,5-dichloro-4-(2-hydroxy-ethoxy)-phenyl]-thioureido}-phenyl)-acetamide (0.20 g) in pyridine (2 mL) and tetrahydrofuran (0.5 mL) is added benzoyl chloride (0.08 g) and the mixture is stirred at 0° C. for 1.5 hours. The mixture is then diluted with ethyl acetate, washed successively two times with 2% aqueous hydrochloric acid, once with saturated aqueous sodium chloride, then dried over anhydrous sodium sulfate. After removal of the solvent under reduced pressure the residue is chromatographed over silica gel (5% methanol in dichloromethane is used as the eluant) and product containing fractions are combined, evaporated under reduced pressure, and the residue is recrystallized from acetone-hexanes to provide the desired product as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06403617B1
Source datasetuspto-grants-2002_06
ORD IDord-e883dff545f24e379872de60aa48c10f
Source noteuspto-grants-2002_06