HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18626Generated: October 25, 2026
Diclofenac → 4-Carbamoylphenyl 2-[2-(2,6-dichlorophenylamino)-phenyl]acetate
https://huagongshe.com/reaction/18626
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diclofenac | HCID 3033 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 4-Hydroxybenzamide | HCID 65052 | — |
| Reactant | HCID 178418300 | HCID 178418300 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Carbamoylphenyl 2-[2-(2,6-dichlorophenylamino)-phenyl]acetate | HCID 59345591 | 17% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07741359B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-efdd765be6a748e18147c7442f20519c |
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| Source note | uspto-grants-2010_06 |
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