HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Butyl iodide → 2',3'-Di-n-butoxy-2,6-dichloro-4'-methoxy-6'-methyl-benzophenone
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Butyl iodide | HCID 10962 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 2,6-Dichloro-2',3'-dihydroxy-4'-methoxy-6'-methyl-benzophenone | HCID 54569551 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 2',3'-Di-n-butoxy-2,6-dichloro-4'-methoxy-6'-methyl-benzophenone | HCID 53713925 | — |
Reaktionsbedingungen
| Temperatur | 100 °C |
|---|
Reaktionsschritte
Sodiumhydride (0.4 g; 60%; 10 mmol) is added with stirring to a solution of 2,6-dichloro-2',3'-dihydroxy-4'-methoxy-6'-methyl-benzophenone (1.64 g; 5 mmol) in tetrahydrofurane. The solvent is evaporated and the residue dissolved in 30 ml of dimethylformamide. 1-iodo-n-butane (4.6 g; 25 mmol) is added, the mixture is stirred at 100° C. for 8 hours and then the solvent is evaporated. The residue is shaken with toluene/2N hydrochloric acid, the organic layer separated, washed with water and the solvent evaporated. The residue is purified by chromatography (flash column filled with 35 g of silicagel; elution with 500 ml of petrolether containing 2% of ethylacetate); yellow oil (0.7 g; 32% y).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05773663 |
| Quelldatensatz | uspto-grants-1998_06 |
| ORD ID | ord-1c3f43f7342345d3bbb71eabe79c1ab1 |
| Quellennotiz | uspto-grants-1998_06 |