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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 443983Erstellt: 25. Oktober 2026

Phenylacetonitrile → trans-3-(beta-Cyanostyryl)-2,2-dimethyl-cyclopropanecarboxylic acid

https://huagongshe.com/reaction/443983

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenylacetonitrileHCID 8794—
EduktEthyl 3-formyl-2,2-dimethylcyclopropane-1-carboxylateHCID 566079—
EduktSodium ethoxideHCID 2723922—
LösungsmittelEthanolHCID 702—
Produkttrans-3-(beta-Cyanostyryl)-2,2-dimethyl-cyclopropanecarboxylic acidHCID 86737697—

Reaktionsschritte

Phenylacetonitrile is added to a stirred solution of sodium ethoxide in absolute ethanol (prepared from 1.1 g sodium and 100 ml of ethanol). Next, a solution of 3-formyl-2,2-dimethyl-cyclopropanecarboxylic acid ethyl ester (8.5 g) in absolute ethanol (15 ml) is added over 5 minutes. The reaction mixture is stirred for 12 hours at room temperature and then heated on a steam bath for 0.5 hour. The alcohol is removed in vacuo, and the residue washed with water (250 ml) and ether (150 ml). The aqueous layer is acidified with concentrated hydrochloric acid. The resulting cream colored slurry is filtered and the isolated product dried. The product is dissolved in ether and precipitated with hexane to afford 6.1 g of white crystals, m.p. 186°-188° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04262117
Quelldatensatzuspto-grants-1981_04
ORD IDord-1e4f110c222d42fdb55abe6645faa667
Quellennotizuspto-grants-1981_04