HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Hydrochloric Acid → 3'-Chloro-4'-fluoroacetophenone
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Acetyl chloride | HCID 6367 | — |
| Edukt | 1-Chloro-2-fluorobenzene | HCID 9583 | — |
| Edukt | 3-Chloro-4-fluorobenzoyl Chloride | HCID 2736548 | — |
| Edukt | Aluminum(III) Chloride | HCID 6451240 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Lösungsmittel | Carbon Disulfide | HCID 6348 | — |
| Lösungsmittel | Tetrachloroethylene | HCID 31373 | — |
| Produkt | 3'-Chloro-4'-fluoroacetophenone | HCID 520422 | 80% |
Reaktionsschritte
3-Chloro-4-fluorobenzoyl chloride is available via a multi-stage synthesis. According to Diep et al., J. Chem. Soc. [1963], 2784-2787, ortho-chlorofluorobenzene is initially reacted with acetyl chloride in the presence of large amounts of aluminum chloride in the presence of carbon disulfide, methylene chloride or tetrachloroethylene, the reaction mixture is decomposed with dilute hydrochloric acid, the organic phase is washed with aqueous sodium hydroxide, then with water, and dried over sodium sulfate, the solvent is evaporated, and the residue is subjected to fractional distillation at reduced pressure. This method gives 3-chloro-4-fluoroacetophenone in a yield of about 80%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06187952B1 |
| Quelldatensatz | uspto-grants-2001_02 |
| ORD ID | ord-f9495f7508b342e992643886567fff12 |
| Quellennotiz | uspto-grants-2001_02 |