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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 417666Erstellt: 24. Oktober 2026

Dimethylcarbamoyl Chloride → Dimethylcarbamoyloxy-phenyl-acetic acid

https://huagongshe.com/de/reaction/417666

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylcarbamoyl ChlorideHCID 6598—
Edukt(+-)-Methyl mandelateHCID 78066—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
ProduktDimethylcarbamoyloxy-phenyl-acetic acidHCID 6662114083%

Reaktionsschritte

To hydroxyl-phenyl-acetic acid methyl ester (500 mg) in THF (10 mL) were added dimethylcarbamoyl chloride (304 μl), TEA (503 μl), and DMAP (37 mg). After stirring for overnight at room temperature, the mixture was taken up in ethyl acetate (150 mL). The organic phase was washed with 1 N HCl (1×100 mL) and saturated sodium bicarbonate (1×100 mL), and dried over sodium sulfate. After the solvent was removed, the resulting solid was dissolved in THF (6 mL). To the solution was added 2 M LiOH (3 mL). After stirring for 90 min. at room temperature, the reaction mixture was acidified with 2 N HCl (3.2 mL). The mixture was extracted with ethyl acetate (50 mL). The organic phase was dried over sodium sulfate. The solvent was removed under reduced pressure to provide dimethylcarbamoyloxy-phenyl-acetic acid (561 mg, 83%) as an off-white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08088368B2
Quelldatensatzuspto-grants-2012_01
ORD IDord-db9e64cf19b148229f5e0e24181eb033
Quellennotizuspto-grants-2012_01