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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 635542Erstellt: 25. Oktober 2026

Hydrochloric Acid → 3'-Chloro-4'-fluoroacetophenone

https://huagongshe.com/reaction/635542

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktAcetyl chlorideHCID 6367—
Edukt1-Chloro-2-fluorobenzeneHCID 9583—
Edukt3-Chloro-4-fluorobenzoyl ChlorideHCID 2736548—
EduktAluminum(III) ChlorideHCID 6451240—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelCarbon DisulfideHCID 6348—
LösungsmittelTetrachloroethyleneHCID 31373—
Produkt3'-Chloro-4'-fluoroacetophenoneHCID 52042280%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06187952B1
Quelldatensatzuspto-grants-2001_02
ORD IDord-f9495f7508b342e992643886567fff12
Quellennotizuspto-grants-2001_02