HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Ammonia → 4-(2-Fluorophenyl)-4-phenylbutanoicacid
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Ammonia | HCID 222 | — |
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | 3-Bromopropionic acid | HCID 11553 | — |
| Edukt | 2-Fluorodiphenylmethane | HCID 138053 | — |
| Edukt | Sodium | HCID 5360545 | — |
| Katalysator | Ferric nitrate | HCID 25251 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | 4-(2-Fluorophenyl)-4-phenylbutanoicacid | HCID 20450025 | — |
Reaktionsschritte
100 g of 2-fluorodiphenylmethane are slowly added dropwise to a solution of sodiuum amide which has been prepared from 500 ml of liquid ammonia, 0.22 g of iron (III) nitrate and 13.2 g of sodium. After 10 minutes, a solution of 40.75 g of 3-bromopropionic acid in 500 ml of ether is added dropwise. After a further 15 minutes, the ammonia is allowed to distill off. The crystallized-out sodium salt of 4-(2-fluorophenyl)-4-phenylbutyric acid is filtered off and washed with ether. The free acid is obtained by treating the sodium salt with dilute hydrochloric acid, extracting the mixture with ether and evaporating the ethereal solution. There is obtained 4-(2-fluorophenyl)-4-phenylbutyric acid of melting point 105°.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04464300 |
| Quelldatensatz | uspto-grants-1984_08 |
| ORD ID | ord-deef2fb43cb5454fa132c07bd98a3f18 |
| Quellennotiz | uspto-grants-1984_08 |