HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1879074Generated: October 25, 2026
Aspirin → 4-Carbamoylphenyl 2-acetoxybenzoate
https://huagongshe.com/reaction/1879074
Participants
| Role | Name | HCID | Charge |
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| Reactant | Aspirin | HCID 2244 | — |
| 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-acetoxybenzoate | HCID 59345592 | 47% |
Reaction Steps
To the solution of 1 (acetylsalicylic acid, 500 mg, 2.77 mmol) in 15 mL of dimethylformamide, hydroxybenzotriazole (412 mg, 3.05 mmol) and DCC (628 mg, 3.05 mmol) were added with stirring at 0° C. for 1 h. To the reaction mixture 4-hydroxybenzamide (4, 418 mg, 3.05 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 to remove the solvent. 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-acetoxybenzoate (5) was obtained (410 mg, 47% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08314140B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-bc49c70413f04fe580fe4a1df29a9023 |
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| Source note | uspto-grants-2012_11 |
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