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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2086916Generated: November 1, 2026

Benzoyl chloride → HCID 86585975, compound

https://huagongshe.com/reaction/2086916

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
Reactant6326-22-3HCID 2796950—
SolventPyridineHCID 1049—
ProductHCID 86585975HCID 8658597546%

Reaction Steps

5-(3,4-dichlorophenylmethylene)-4-oxo-2-thionothiazolidine (100 mg, 0.345 mmol, 1.0equiv) was suspended in 653 μL of anhydrous pyridine, followed by the addition of 44 μL benzoyl chloride (0.379 mmol, 1.1 equiv). After about 2 minutes a yellow precipitate formed. The reaction was stirred at rt for 30 minutes. The pyridine was evaporated and the residue was purified by column chromatography (SiO2, EtOAc/hexanes) to yield 62 mg of 5-(3,4-dichlorophenylmethylene)-3-(benzoyl)-4-oxo-2-thionothiazolidine (0.157 mmol, 46%) as a yellow solid. Anal. calcd for C17H9Cl2NO2S2: C, 51.78; H, 2.30; N, 3.55; S, 16.26. Found: C, 52.04; H, 2.47; N, 3.48; S, 16.26.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06727267B2
Source datasetuspto-grants-2004_04
ORD IDord-e49f571b25af42cfb069b68fecc09756
Source noteuspto-grants-2004_04