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HRID 44170Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/44170

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiclofenacHCID 3033—
EduktDicyclohexylcarbodiimideHCID 10868—
EduktDesmethylanethol trithioneHCID 3082127—
EduktHCID 178418300HCID 178418300—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
Produkt4-Isothiocyanatophenyl 2-(2-(2,6-dichlorophenylamino)phenyl)acetateHCID 2506577023%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08541398B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-206a10ec26d64b0c904bc790354ed986
Quellennotizuspto-grants-2013_09