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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2187706Generated: October 30, 2026

Benzoyl chloride → HCID 53746038, compound

https://huagongshe.com/reaction/2187706

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 numberUS06410571B1
Source datasetuspto-grants-2002_06
ORD IDord-ed9bdc79faf54aba9d5fadf3b6ed47f2
Source noteuspto-grants-2002_06