HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2112051Erstellt: 25. Oktober 2026
Potassium Hydroxide → 2-[(4-{2-[Heptyl(2-phenylethyl)amino]-2-oxoethyl}-phenoxy)methyl]benzoic acid
https://huagongshe.com/reaction/2112051
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | Methyl 2-[(4-{2-[heptyl(2-phenylethyl)amino]-2-oxoethyl}phenoxy)methyl]-benzoate | HCID 68869824 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 2-[(4-{2-[Heptyl(2-phenylethyl)amino]-2-oxoethyl}-phenoxy)methyl]benzoic acid | HCID 10458165 | 30,3% |
Reaktionsschritte
Methyl 2-[(4-{2-[heptyl(2-phenylethyl)amino]-2-oxoethyl}phenoxy)methyl]benzoate (0.146 g, 0.291 mmol) was dissolved in EtOH (5 ml, 95%), potassium hydroxide (0.025 g, 0.437 mmol) was added. The reaction was performed in an single node microwave oven (7 min, 150° C.). Work-up was by removing the solvent by evaporation and addition of HCl (2 ml, 1 M). The water-phase was extracted with two portions of EtOAc (20 ml) and the organic phase was dried (MgSO4) and the solvent was removed by evaporation. The crude was purified by preparative HPLC (started with isocratic acetonitrile/buffer 60/40 and then the acetonitrile concentration was increased to 100%, the buffer was a mixture of acetonitrile/water 10/90 and ammonium acetate (0.1 M, column KR-100-7-C8, 50 mm×250 mm, flow 40 ml/min). The product containing fractions were pooled and the acetonitrile was removed by evaporation EtOAc (10 ml) was added and the organic phase was washed with two portions of brine and dried (MgSO4). The solvent was removed by evaporation to give 0.043 g of 2-[(4-{2-[heptyl(2-phenylethyl)amino]-2-oxoethyl}-phenoxy)methyl]benzoic acid (yield 30.3%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07521461B2 |
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| Quelldatensatz | uspto-grants-2009_04 |
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| ORD ID | ord-344ff2ade96445399e267108422d9551 |
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| Quellennotiz | uspto-grants-2009_04 |
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