HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
2-Ethylbutyraldehyde → 2-(4-Chlorobenzyl)-2-ethylbutanal
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 2-Ethylbutyraldehyde | HCID 7359 | — |
| Edukt | 1-Chloro-4-(chloromethyl)benzene | HCID 7723 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Katalysator | Tetrabutylammonium Iodide | HCID 67553 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 2-(4-Chlorobenzyl)-2-ethylbutanal | HCID 15100831 | — |
Reaktionsschritte
300 ml of toluene, 400 ml of 30 percent (by weight) sodium hydroxide solution and 5.0 g of tetra-n-butyl-ammonium iodide are heated at 80° C. while stirring. To this is slowly added dropwise a mixture of 110 g (1.10 mol) of 2-ethylbutanal and 161 g (1.00 mol) of 4-chlorobenzyl chloride. The mixture is then stirred at 80° C. for 4 h and at room temperature for 14 h, 1,000 ml of toluene are added, and the phases are separated. The organic phase is washed with water, dried over Na2SO4 and concentrated. Fractional distillation results in 123 g (54% of theory) of 2-(4-chlorobenzyl) -2-ethylbutanal as a colorless liquid of boiling point 146°-148° C. at 1 mbar.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05266579 |
| Quelldatensatz | uspto-grants-1993_11 |
| ORD ID | ord-b9ac554c1e4446a69a6e51b89084bc63 |
| Quellennotiz | uspto-grants-1993_11 |