HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1416086Erstellt: 26. Oktober 2026
Oxygen → (S)-2-(4-Fluorophenyl)-3-methylbutyric acid
https://huagongshe.com/reaction/1416086
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Oxygen | HCID 977 | — |
| Edukt | 3-Methyl-2-(p-fluorophenyl)crotonic acid | HCID 11019724 | — |
| Katalysator | Ruthenium | HCID 23950 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | (S)-2-(4-Fluorophenyl)-3-methylbutyric acid | HCID 11112309 | 97,5% |
Reaktionsschritte
Ruthenium-catalyzed hydrogenation. -- A catalyst solution was prepared in a glove box (O2 content <1 ppm) by dissolving 0.418 g (0.544 mmol) of Ru(OAc)2 [(R)-BlPHEMP] in 100 ml of methanol and stirring at RT for 10 minutes. Then, 211.2 g (1.0875 mol) of 2-(p-fluorophenyl)-3-methylcrotonic acid and 700 ml of methanol were placed in a 2 l autoclave and the catalyst solution prepared above was added. The autoclave was sealed and the hydrogenation was carried out while stirring at 10° and under a pressure of 150-180 bar. The conversion was 100% after 24 hours. The hydrogenation solution was evaporated at 50°/200 mbar and the residue was distilled at 108-110°/ 0.01 mbar. There were obtained 208.1 g (97.5%) of (S)-2-(p-fluorophenyl)-3-methylbutyric acid as a colorless oil which solidified at RT; m.p. 53-56°; 96.6% ee.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US05910606 |
|---|
| Quelldatensatz | uspto-grants-1999_06 |
|---|
| ORD ID | ord-25229741784c49c492f2924a31261f48 |
|---|
| Quellennotiz | uspto-grants-1999_06 |
|---|