HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
2-Chlorophenol → Ethyl 2-(2-chlorophenoxy)acetate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 2-Chlorophenol | HCID 7245 | — |
| Edukt | Ethyl bromoacetate | HCID 7748 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Produkt | Ethyl 2-(2-chlorophenoxy)acetate | HCID 302826 | 95% |
Reaktionsschritte
To a stirred solution of 2-chlorophenol (6, 20.0 g, 156 mmol) in acetone (300 mL) under nitrogen at ambient temperature were added potassium carbonate (23.7 g, 171 mmol) and ethyl bromoacetate (7, 26.0 g, 156 mmol). The reaction mixture was then heated to reflux and stirred at this temperature under nitrogen for 7 hours. After cooling to ambient temperature, the reaction mixture was filtered to remove insolubles. The filtrate was then concentrated under reduced pressure to give 8 as highly viscous, light yellow oil (32.0 g, 95% yield, 95% pure by LCMS and 1H NMR), 1H NMR (400 MHz; CDCl3): δ 7.16 (m, 1H); 7.03 (m, 1H); 6.76 (m, 1H); 6.71 (m, 1H); 4.90 (s, 2H); 4.12 (q, 2H); 1.33 (t, 3H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07098211B2 |
| Quelldatensatz | uspto-grants-2006_08 |
| ORD ID | ord-5026b40714514b03bf4016e828417bd4 |
| Quellennotiz | uspto-grants-2006_08 |