HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 417666Erstellt: 24. Oktober 2026
Dimethylcarbamoyl Chloride → Dimethylcarbamoyloxy-phenyl-acetic acid
https://huagongshe.com/de/reaction/417666
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Dimethylcarbamoyl Chloride | HCID 6598 | — |
| Edukt | (+-)-Methyl mandelate | HCID 78066 | — |
| Katalysator | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | Dimethylcarbamoyloxy-phenyl-acetic acid | HCID 66621140 | 83% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08088368B2 |
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| Quelldatensatz | uspto-grants-2012_01 |
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| ORD ID | ord-db9e64cf19b148229f5e0e24181eb033 |
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| Quellennotiz | uspto-grants-2012_01 |
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