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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 44170Generated: October 26, 2026

Diclofenac → 4-Isothiocyanatophenyl 2-(2-(2,6-dichlorophenylamino)phenyl)acetate

https://huagongshe.com/reaction/44170

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiclofenacHCID 3033—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantDesmethylanethol trithioneHCID 3082127—
ReactantHCID 178418300HCID 178418300—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product4-Isothiocyanatophenyl 2-(2-(2,6-dichlorophenylamino)phenyl)acetateHCID 2506577023%

Reaction Conditions

Temperature0 °C

Reaction Steps

To the solution of 1 (diclofenac, 1717 mg, 5.8 mmol) in 60 mL of dimethylformamide, hydroxybenzotriazole (862 mg, 6.38 mmol) and DCC (1316 mg, 6.38 mmol) were added with stirring at 0° C. for 1 h. To the reaction mixture 4-hydroxyphenylisothiocyanate (2; 965 mg, 6.38 mmol) was added and stirred for 1 h at 0° C. and 2 h at room temperature. After filtration, the filtrate was evaporated under reduced pressure to remove the solvent. The oily residue thus obtained was dissolved in ethyl acetate and the precipitate was removed. The solvent was evaporated and the crude product was loaded on a silica gel open column and eluted with chloroform/n-hexane 9:1, from which 4-isothiocyanatophenyl 2-(2-(2,6-dichlorophenylamino)phenyl)acetate (3) was obtained (580 mg, 23% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541398B2
Source datasetuspto-grants-2013_09
ORD IDord-206a10ec26d64b0c904bc790354ed986
Source noteuspto-grants-2013_09