HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2242922Generated: October 26, 2026
Ibuprofenamide → 2-(4-Isobutylphenyl)propiononitrile
https://huagongshe.com/reaction/2242922
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ibuprofenamide | HCID 101072 | — |
| Reactant | Phosgen toluene | HCID 19083224 | — |
| Solvent | Toluene trichloromethane | HCID 22987606 | — |
| Product | 2-(4-Isobutylphenyl)propiononitrile | HCID 108374 | 80% |
Reaction Steps
4-isobutyl-α-methylphenylacetamide (2 g; 9.7 mmol), prepared according the procedure described in WO 00/24710, is dissolved in a solution (2:1) toluene/trichloromethane (30 mL). 20% in toluene phosgene (15.5 mL, 30 mmol) is added and the resulting mixture is left stirring 12 h under inert atmosphere until the complete disappearance of the starting reagent. After solvents evaporation under reduced pressure, the crude is dissolved in ethyl acetate (20 mL), the organic phase is washed with a saturated solution of NaHCO3 (2×20 mL) and with a saturated solution of NaCl (2×15 mL), dried over Na2SO4 and evaporated under vacuum to give 2-(4-isobutylphenyl)propionitrile as colourless oil (1.45 g; 7.76 mmol). Yield 80%. 1H-NMR (CDCl3): δ 7.42 (d, 2H, J=7 Hz); 7.28 (d, 2H, J=7 Hz); 4.05 (q, 1H, J=8 Hz); 2.65 (d, 2H, J=8 Hz); 1.95 (m, 1H); 1.80 (d, 3H, J=8 Hz); 1.05 (d, 6H, J=8 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07674806B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-d4445f8854d54a9997cff64c9f09902d |
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| Source note | uspto-grants-2010_03 |
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