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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2299712Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/2299712

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
PatentnummerUS06495581B1
Quelldatensatzuspto-grants-2002_12
ORD IDord-20613cfbb7604198840da3b3eac470b1
Quellennotizuspto-grants-2002_12