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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 362269Erstellt: 25. Oktober 2026

Potassium Hydroxide → 4-(4-Phenoxybut-2-ynylthio)benzonitrile

https://huagongshe.com/reaction/362269

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium HydroxideHCID 14797—
Edukt4-ThiobenzonitrileHCID 585058—
Edukt1-Chloro-4-phenoxybut-2-yneHCID 10943069—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
Produkt4-(4-Phenoxybut-2-ynylthio)benzonitrileHCID 54508157—

Reaktionsschritte

A solution of potassium hydroxide (7.5 g) in a mixture of ethanol (220 ml) and water (55 ml) was added at ambient temperature under nitrogen to a stirred solution of 4-mercaptobenzonitrile (18.0 g; prepared according to the method of S. Krishnamurthy and D. Aimino, J. Org. Chem., 1989, 54, 4458) in a mixture of ethanol (195 ml) and water (12 ml), then the mixture was stirred at ambient temperature for 4.5 hours. A solution of 1-chloro-4-phenoxybut-2-yne (24.1 g; prepared in a similar manner to that described in Example 5) in a mixture of ethanol (195 ml) and water (12 ml) was added dropwise over 1.5 hours, then the mixture was stirred at ambient temperature for 17 hours. The mixture was concentrated in vacuo to remove the ethanol, then the product was diluted with water (150 ml) and extracted into ethyl acetate (2×250 ml). The combined extracts were washed with water (100 ml) and saturated brine (100 ml), dried (MgSO4), and the solvent removed in vacuo to leave 4-(4-phenoxybut-2-ynylthio)benzonitrile as an off-white solid (37.7 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05869492
Quelldatensatzuspto-grants-1999_02
ORD IDord-a805daa329c6473aafeb2d7e69fddb35
Quellennotizuspto-grants-1999_02