Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methanol | HCID 887 | — |
| Edukt | Thionyl Chloride | HCID 24386 | — |
| Edukt | 4-Bromo-2,2-diphenylbutyric acid | HCID 2756959 | — |
| Katalysator | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Produkt | Methyl 4-bromo-2,2-diphenylbutyrate | HCID 22624494 | — |
Reaktionsschritte
4-Bromo-2,2-diphenylbutyric acid (5.0 g, 16 mmol), thionyl chloride (1.1 mL, 16 mmol), and N,N-dimethylformamide (0.02 mL, 0.20 mmol) in chloroform (16 mL) were mixed at room temperature under a stream of nitrogen. The reaction mixture was heated to reflux, stirred under reflux for 4 h, and cooled to 0° C. Methanol (50 mL) was added. The reaction mixture was warmed to room temperature and concentrated to dryness, yielding a brown oil. The crude material was purified on SiO2 (120 g) using 10% EtOAc/Hexanes as eluent to provide the title compound (3.9 g) as a clear oil that crystallized on standing. 1H NMR (DMSO-d6, 400 mHz) δ (ppm): 7.33-7.20 (m, 10H), 3.70 (s, 3H), 3.12-3.08 (m, 2H), 2.98-2.93 (m, 2H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US08101791B2 |
|---|
| Quelldatensatz | uspto-grants-2012_01 |
|---|
| ORD ID | ord-9aef0e17953e41e5bb111cd38c7aa214 |
|---|
| Quellennotiz | uspto-grants-2012_01 |
|---|