HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Potassium Hydroxide → 3-[(4-Fluorophenyl)thio]-2-hydroxy-2-methylpropanoic acid
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 4-Fluorothiophenol | HCID 67789 | — |
| Edukt | Methyl 2-hydroxy-2-methyl-3-(4-fluorophenylthio)-propionate | HCID 21966928 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 3-[(4-Fluorophenyl)thio]-2-hydroxy-2-methylpropanoic acid | HCID 9813367 | — |
Reaktionsschritte
The methyl 2-methyl-oxirane-carboxylate of formula (1), which was obtained by epoxidation, was reacted with 4-fluorothiophenol [formula (2)] in the presence of sodium hydride under the conditions listed in Scheme-2. The obtained methyl 2-hydroxy-2-methyl-3-(4-fluorophenylthio)-propionate of formula (3) was hydrolyzed with potassium hydroxide in aqueous ethanol over a period of 22 hours to yield the 2-hydroxy-2-methyl-3-(4-fluorophenylthio)-propionic acid of formula (4), which was converted into acid chloride of formula (5) with thionyl chloride in dimethyl acetamide at −15° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07102026B2 |
| Quelldatensatz | uspto-grants-2006_09 |
| ORD ID | ord-c604cc732ca64c99b9765e91bfb0a4be |
| Quellennotiz | uspto-grants-2006_09 |