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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 44160Generated: October 26, 2026

Diclofenac → S-Diclofenac

https://huagongshe.com/reaction/44160

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiclofenacHCID 3033—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantDesmethylanethol trithioneHCID 3082127—
ReactantHCID 178418300HCID 178418300—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductS-DiclofenacHCID 1194830774%

Reaction Conditions

Temperature0 °C

Reaction Steps

To the solution of 1 (diclofenac, 890 mg, 3.0 mmol) in 50 mL of N,N-dimethylformamide, hydroxybenzotriazole (445 mg, 3.3 mmol) and DCC (680 mg, 3.3 mmol) were added with stirring at 0° C. for 1 h. To the reaction mixture 5-p-hydroxyphenyl-1,2-dithiole-3-thione (2; 678 mg, 3 mmol) was added and stirred for 1 h at 0° C. and 3 h at room temperature. After filtration, the filtrate was evaporated under reduced pressure and the oily residue thus obtained was dissolved in ethyl acetate; the organic layer was washed with brine, dried on anhydrous MgSO4, filtered and the solvent evaporated. The crude product 3 was loaded on a silica gel open column and eluted with CH2Cl2/MeOH (9/1), from which [2-(2,6-dichloro-phenylamino)-phenyl]-acetic acid 4-(5-thioxo-5H-[1,2]dithiol-3-yl)-phenyl ester (3) was obtained (1.1 g, 74% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541398B2
Source datasetuspto-grants-2013_09
ORD IDord-524b1f6b99df4db48a59db8265a7f4eb
Source noteuspto-grants-2013_09