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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1379249Erstellt: 25. Oktober 2026

3-Chlorobenzoic Acid → 3-Chlorobenzoic Acid

https://huagongshe.com/reaction/1379249

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Chlorobenzoic AcidHCID 447—
Eduktm-Chloroperbenzoic acidHCID 70297—
Edukt2-OxocyclohexanepropiononitrileHCID 96223—
LösungsmittelHexaneHCID 8058—
Produkt3-Chlorobenzoic AcidHCID 447—
Produkt3-(7-Oxooxepan-2-yl)propanenitrileHCID 11768938—

Reaktionsbedingungen

Temperatur55 °C

Reaktionsschritte

A reactor is loaded with 151 g of 3-(2-cyclohexanonyl)propionitrile in 500 ml of n-hexane and 260 g of m-chloroperbenzoic acid (70% titer) dissolved at 50° C. in 2000 ml of n-hexane in 30 minutes. The solution is heated to 55° C. for 15 hours. Cooling separates from the solution, in crystalline form, part of the m-chlorobenzoic acid, which is scarcely soluble in the system, together with a heavy liquid phase which is formed by 7-cyanoethyl-2-oxepanone and by m-chlorobenzoic acid. 71.5 g of 7-cyanoethyl-2-oxepanone, impure with m-chlorobenzoic acid, are recovered from the lower phase. 24 g of 7-cyanoethyl-2-oxepanone are recovered from the upper phase by concentration and by several crystallizations. Conversion with respect to the initial ketone is 85%. Yield on the converted substance is 57%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05670661
Quelldatensatzuspto-grants-1997_09
ORD IDord-62b2e574547047a89abd0f996fcfb47e
Quellennotizuspto-grants-1997_09