HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 430720Erstellt: 24. Oktober 2026
Sodium Hydroxide → 2-Hydroxy-3-methyl-4-oxo-4-(3',4'-dichlorophenyl)butanoic acid
https://huagongshe.com/de/reaction/430720
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 3',4'-Dichloropropiophenone | HCID 81060 | — |
| Edukt | Glyoxylic acid, monohydrate | HCID 15620607 | — |
| Edukt | Dichloromethane methanol | HCID 21226129 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Diethylether hexane | HCID 21584099 | — |
| Produkt | 2-Hydroxy-3-methyl-4-oxo-4-(3',4'-dichlorophenyl)butanoic acid | HCID 10039146 | 27% |
Reaktionsschritte
To a solution of 1-(3,4-dichlorophenyl)propanone (5.8 g, 28.5 mmol)in 95% ethanol (100 mL) a solution of glyoxylic acid monohydrate (2.63 g, 28.5 mmol) in water (20 mL) was added at 0° C., followed by dropwise addition of a solution of sodium hydroxide (4.6 g, 0.114 mol). The temperature during the addition was maintained below +5° C. on cooling. The resulting reaction mixture was stirred at 0° C. over 3 hours, then allowed to warm to room temperature and stirred further 12 hours. The most of ethanol was then removed under reduced pressure (15° C.), the residue was diluted with water and the pH of the obtained suspension adjusted to 2 by addition of 37% HCl, on stirring and cooling at 0° C. The aqueous phase was extracted with ethyl acetate, and the collected organic extracts were washed with brine, dried and evaporated to provide the crude reaction product as a light yellow oil (4.4 g). Column chromatography (SiO2; CH2Cl2/MeOH 95:5) provided the pure titled compound (2.1 g, 27%), colorless solid (Ethyl ether/hexane) mp. 103-104° C.;
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06323240B1 |
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| Quelldatensatz | uspto-grants-2001_11 |
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| ORD ID | ord-d14c65e9109f43f5ba3b2ca71822351a |
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| Quellennotiz | uspto-grants-2001_11 |
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