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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18633Generated: October 25, 2026

Ibuprofen, (+-)- → 4-Thiocarbamoylphenyl 2-(4-isobutylphenyl)propanoate

https://huagongshe.com/reaction/18633

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIbuprofen, (+-)-HCID 3672—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantDesmethylanethol trithioneHCID 3082127—
ReactantHCID 178418300HCID 178418300—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product4-Thiocarbamoylphenyl 2-(4-isobutylphenyl)propanoateHCID 2506576840%

Reaction Conditions

Temperature0 °C

Reaction Steps

To the solution of 1 (ibuprofen, 3.87 g, 18.8 mmol) in 80 mL of dimethylformamide, hydroxybenzotriazole (2.8 g, 20.7 mmol) and DCC (4.27 g, 20.7 mmol) were added with stirring at 0° C. for 1 h. To the reaction mixture 4-hydroxybenzamide (2, 3.9 g, 28 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; the organic layer was washed with brine, with NaHCO3 5%, with citric acid 10% and than dried on anhydrous MgSO4, filtered and the solvent evaporated. The crude product 3 was loaded on a silica gel open column and eluted with CH2Cl2/MeOH (9.5/0.5), from which 4-carbamoylphenyl 2-(4-isobutylphenyl)propanoate (3) was obtained (2.48 g, 40% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741359B2
Source datasetuspto-grants-2010_06
ORD IDord-1ca9112d08974993bf3da659e149b590
Source noteuspto-grants-2010_06