HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Benzyl Bromide → 2-(Benzyloxy)-3-methoxybenzaldehyde
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Benzyl Bromide | HCID 7498 | — |
| Edukt | o-Vanillin | HCID 8991 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 2-(Benzyloxy)-3-methoxybenzaldehyde | HCID 1268087 | 93% |
Reaktionsschritte
A mixture of 196.0 g (1.30 mole) of o-vanillin (Aldrich), 200 g of benzyl bromide (Aldrich), 500 g of anhydrous potassium carbonate and 1,500 mL of absolute ethanol is heated, with stirring, at reflux for 6 hours. After cooling, the supernatant is decanted and the remainder is filtered. The combined filtrate and supernatant is concentrated at reduced pressure to remove solvent. The remaining oil is extracted into 1 L of ether. The ether solution is washed with 500 mL of water, 600 mL of 1% potassium hydroxide solution, and 500 mL of water and then dried (potassium carbonate) and concentrated to give 263.4 g (84% yield) of product; mp 41°-43° C. Reported mp, 43° C. (Chem. Abstr. 62:16110a).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05246943 |
| Quelldatensatz | uspto-grants-1993_09 |
| ORD ID | ord-0b20c9191db0436d9a89e14bbc14aaef |
| Quellennotiz | uspto-grants-1993_09 |