HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Potassium Iodide → Potassium Hydroxide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Potassium Iodide | HCID 4875 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Bromocyclobutane | HCID 78110 | — |
| Edukt | 4-Cyclopropoxybenzoic acid | HCID 21452864 | — |
| Edukt | Ethyl 4-cyclobutyloxybenzoate | HCID 21452944 | — |
| Edukt | 2-Ethyl-4-hydroxybenzamide | HCID 21453012 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | Potassium Hydroxide | HCID 14797 | 10% |
| Produkt | 4-Cyclobutoxybenzoic acid | HCID 21452881 | — |
Reaktionsschritte
The intermediate 4-cyclobutyloxybenzoic acid was prepared following the procedure described in Example 108 for the preparation of the corresponding 4 -cyclopropyloxybenzoic acid using 25 g. of ethyl 4-hydroxybenzamide, 23.1 g. of cyclobutyl bromide, 31 g. of anhydrous potassium carbonate, 2.5 g. of potassium iodide and 300 ml. of dimethylformamide to yield 20.1 g. of ethyl 4-cyclobutyloxybenzoate, which was then hydrolyzed by heating with 200 ml. of 10% aqueous potassium hydroxide solution as in Example 108 to yield 12.7 g. of 4-cyclobutyloxybenzoic acid, m.p. 192°-195° C. after recrystallization from 400 ml. of acetonitrile.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04009208 |
| Quelldatensatz | uspto-grants-1977_02 |
| ORD ID | ord-412f674b2e844eccb0a5302d1e76cbd2 |
| Quellennotiz | uspto-grants-1977_02 |