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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 616756Erstellt: 23. Oktober 2026

Ammonia → 3-Chloro-4-cyclohexylethynylbenzene

https://huagongshe.com/de/reaction/616756

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmoniaHCID 222—
EduktSodium amideHCID 24533—
EduktPhosphorus pentachlorideHCID 24819—
Edukt3-Chloro-4-cyclohexylacetophenoneHCID 56975890—
LösungsmittelWaterHCID 962—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-Chloro-4-cyclohexylethynylbenzeneHCID 57286755—

Reaktionsschritte

3-Chloro-4-cyclohexylacetophenone (0.25 moles) and phosphorus pentachloride (0.31 moles) are placed in a 3-necked flask equipped with a mechanical stirrer, a condenser connected to a nitrogen inlet, and a thermometer. The mixture is stirred at 33°-35° C for 3 days. The cooled reaction mixture is poured onto 800 g. of ice and extracted with 3 × 500 ml. of ether. The ether fraction is washed with 2 × 100 ml water 4 × 100 ml of 5% sodium hydroxide, 3 × 50 ml water, 2 × 50 ml of saturated saline and dried over sodium sulfate. The ether is removed to give the chlorinated intermediate. The intermediate is dissolved in anhydrous THF (200 ml) and is added dropwise to a freshly prepared solution of sodamide in liquid ammonia, using a dry-ice condenser. The reaction mixture is allowed to stir at room temperature overnight; then, it is poured into 50 ml of water and 500 ml of ether. The ether fraction is washed with 3 × 50 ml water and 50 ml of saturated saline and is dried over sodium sulfate. Removal of solvent gives a residue which is distilled to give 3 -chloro-4-cyclohexylethynylbenzene.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04075354
Quelldatensatzuspto-grants-1978_02
ORD IDord-2ee1aeaec89d46228d533e3d69123fc6
Quellennotizuspto-grants-1978_02