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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 44161Generated: October 26, 2026

Diclofenac → 4-Carbamoylphenyl 2-[2-(2,6-dichlorophenylamino)-phenyl]acetate

https://huagongshe.com/reaction/44161

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiclofenacHCID 3033—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant4-HydroxybenzamideHCID 65052—
ReactantHCID 178418300HCID 178418300—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
Product4-Carbamoylphenyl 2-[2-(2,6-dichlorophenylamino)-phenyl]acetateHCID 5934559117%

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 4-hydroxybenzamide (4, 616 mg, 4.5 mmol) was added and stirred for 1 h at 0° C. and 3 hs at room temperature. After filtration, the filtrate was evaporated under reduced pressure and the oily residue thus obtained was dissolved in chloroform; the organic layer was washed with brine, dried on anhydrous MgSO4, filtered and the solvent evaporated. The crude product 5 was loaded on a silica gel open column and eluted with CH2Cl2/MeOH (9/1), from which 4-carbamoylphenyl 2-(2-(2,6-dichlorophenylamino)phenyl)acetate (5) was obtained (212 mg, 17% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541398B2
Source datasetuspto-grants-2013_09
ORD IDord-e02319aa71c74df7a7d37a8e358774bf
Source noteuspto-grants-2013_09