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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium HydroxideHCID 14797—
EduktMethyl 2-[(4-{2-[heptyl(2-phenylethyl)amino]-2-oxoethyl}phenoxy)methyl]-benzoateHCID 68869824—
LösungsmittelEthanolHCID 702—
Produkt2-[(4-{2-[Heptyl(2-phenylethyl)amino]-2-oxoethyl}-phenoxy)methyl]benzoic acidHCID 1045816530,3%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07521461B2
Quelldatensatzuspto-grants-2009_04
ORD IDord-344ff2ade96445399e267108422d9551
Quellennotizuspto-grants-2009_04