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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1879074Generated: October 25, 2026

Aspirin → 4-Carbamoylphenyl 2-acetoxybenzoate

https://huagongshe.com/reaction/1879074

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAspirinHCID 2244—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant4-HydroxybenzamideHCID 65052—
ReactantHCID 178418300HCID 178418300—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
Product4-Carbamoylphenyl 2-acetoxybenzoateHCID 5934559247%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314140B2
Source datasetuspto-grants-2012_11
ORD IDord-bc49c70413f04fe580fe4a1df29a9023
Source noteuspto-grants-2012_11