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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1070038Erstellt: 26. Oktober 2026

Isoamyl Nitrite → 2-Hydroxyimino-2-(3-phenoxyphenyl)acetonitrile

https://huagongshe.com/reaction/1070038

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIsoamyl NitriteHCID 8053—
Eduktm-Phenoxybenzyl cyanideHCID 40075—
EduktSodium ethoxideHCID 2723922—
EduktSodiumHCID 5360545—
LösungsmittelEthanolHCID 702—
LösungsmittelDiethyl EtherHCID 3283—
Produkt2-Hydroxyimino-2-(3-phenoxyphenyl)acetonitrileHCID 8530827945%

Reaktionsschritte

To a solution of sodium ethoxide prepared from sodium (1.09 g) and ethanol (20 ml), a solution of 3-phenoxyphenylacetonitrile (8.30 g) in ethanol (15 ml) was added dropwise at 0° C., and then isoamyl nitrite (7.99 ml) was added dropwise. After stirring for 15 hours at room temperature, diethyl ether was added and the mixture was washed sequentially with 1N HCl, aqueous sodium bicarbonate and then saturated aqueous sodium chloride. The diethyl ether layer was dried (MgSO4), concentrated, and the residue was subjected to column chromatography on silica gel. The crystals obtained from a fraction eluted with ethyl acetate-hexane (1:4, v/v) were recrystallized with ethyl acetate-hexane to obtain 2-hydroxyimino-2-(3-phenoxyphenyl)acetonitrile (4.25 g, yield: 45%) as pale-yellow crystals. A mixture of the E- form and the Z- form. m.p. 124-125° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06251926B1
Quelldatensatzuspto-grants-2001_06
ORD IDord-4315ba764d5148efaf6776f8b73e386d
Quellennotizuspto-grants-2001_06