HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Sodium bis(trimethylsilyl)amide → 3-(3-Cyano-phenyl)-2-methyl-propionic acid methyl ester
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Edukt | Methyl 3-(3-cyanophenyl)propanoate | HCID 20257048 | — |
| Edukt | Sodium bicarbonate water | HCID 86585896 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 3-(3-Cyano-phenyl)-2-methyl-propionic acid methyl ester | HCID 54523024 | 26,3% |
Reaktionsschritte
To a solution of 3-(3-cyano-phenyl)-propionic acid methyl ester of Step A (220 mg, 1.16 mmol) in THF (5 mL) at −78° C. was added sodium bis(trimethylsilyl)amide (1 M in THF, 1.2 mL, 1.2 mmol). The reaction was stirred for 0.5 h and Mel (0.08 mL, 1.28 mmol) was added. After 1 h, a solution of saturated NaHCO3:water (1:1) was added and the reaction was warmed to room temperature. The aqueous solution was washed with CH2Cl2 (3×) and the combined organic solutions were dried (MgSO4), filtered, and concentrated. Medium pressure chromatography (6:1 hexanes:EtOAc) provided the title compound of Step B as a colorless oil (62 mg). 1H NMR (400 MHz, CDCl3) δ 7.50-7.34 (m, 4H), 3.62 (s, 3H), 3.01 (m, 1H), 2.71 (m, 2H), 1.16 (d, 3H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06498172B1 |
| Quelldatensatz | uspto-grants-2002_12 |
| ORD ID | ord-a21535a9dbbe4ef8b90881c0b032750d |
| Quellennotiz | uspto-grants-2002_12 |