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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 867001Erstellt: 26. Oktober 2026

Diethyl Ether → 4-(3-Trifluoromethylbenzoyl)piperidine

https://huagongshe.com/reaction/867001

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl EtherHCID 3283—
EduktBenzene, 1-bromo-3-(trifluoromethyl)-HCID 9817—
EduktAmmonium ChlorideHCID 25517—
Edukt1-Acetylpiperidine-4-carbonitrileHCID 2756286—
EduktMagnesiumHCID 5462224—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-(3-Trifluoromethylbenzoyl)piperidineHCID 5086447—

Reaktionsschritte

4-(3-trifluoromethylbenzoyl)piperidine is prepared in the following manner: A solution of 102.5 g of 3-bromobenzotrifluoride in 25 ml of ether is added dropwise to a stirring mixture of 11.5 g of magnesium turnings in 300 ml of anhydrous ether to maintain a moderate reflux. After total addition the resulting dark mixture is stirred for 1 hour at ambient temperature. A solvent of 60.0 g of 1-acetyl-4-cyanopiperidine in 100 ml of tetrahydrofuran is slowly added to this mixture and the mixture is stirred for 16 hours. An excess of an aqueous solution of ammonium chloride is added and the mixture is heated on a steam bath for 3 hours. The mixture is allowed to cool, extracted with benzene and the combined extracts are dried. The solvent is removed and the residue is dissolved in ethanol and basified with sodium hydroxide. The alkaline solution is refluxed for 3 hours, cooled and extracted with benzene. The combined benzene extracts are dried and the benzene is removed, leaving the oil, 4-(3 -trifluoromethylbenzoyl)piperidine, which is converted to the hydrochloride, mp. 196°-198° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04101663
Quelldatensatzuspto-grants-1978_07
ORD IDord-8bbd513e7d304af486da9f3df2afc6e7
Quellennotizuspto-grants-1978_07