HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2242923Erstellt: 26. Oktober 2026
Hydrochloric Acid → 2-(4-Isobutylphenyl)propionamide hydrochloride
https://huagongshe.com/reaction/2242923
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | 2-(4-Isobutylphenyl)propiononitrile | HCID 108374 | — |
| Edukt | Diethyl ether methanol | HCID 21864698 | — |
| Produkt | 2-(4-Isobutylphenyl)propionamide hydrochloride | HCID 68637298 | 75% |
Reaktionsschritte
A solution of 2-(4-isobutylphenyl)propionitrile (0.2 g; 1.07 mmol) in a (1:1) diethyl ether/methyl alcohol mixture (20 mL) is cooled at T=0-5° C. and gaseous HCl is bubbled into the solution for 1 h. Then the temperature is left to arise to r.t. and the mixture stirred overnight. After solvent evaporation under reduced pressure, the crude is dissolved in methyl alcohol (10 mL) and cooled at T=0-5° C. Ammonia is bubbled into for 1 h and the resulting mixture is left stirring overnight at r.t. After solvent evaporation under reduced pressure, the crude is suspended in diethyl ether (15 mL) and left stirring at r.t. for 2 h. The 2-(4-isobutylphenyl)propionamide hydrochloride (I) is isolated by filtration in vacuo as white solid (0.193 g; 0.80 mmol). Yield 75%. 1H-NMR (DMSO-d6): δ 8.80-8.50 (bs, NH3+Cl−); 7.40 (d, 2H, J=7 Hz); 7.15 (d, 2H, J=7 Hz); 3.98 (q, 1H, J=8 Hz); 2.42 (d, 2H, J=8 Hz); 1.90 (m, 1H); 1.57 (d, 3H, J=8 Hz); 0.88 (d, 6H, J=8 Hz).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07674806B2 |
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| Quelldatensatz | uspto-grants-2010_03 |
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| ORD ID | ord-6e3f75c614bd4ad4b427931e90a184f6 |
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| Quellennotiz | uspto-grants-2010_03 |
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