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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070043Generated: November 1, 2026

Isoamyl Nitrite → 2-(3-Benzoylphenyl)-2-(hydroxyimino)acetonitrile

https://huagongshe.com/reaction/1070043

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsoamyl NitriteHCID 8053—
Reactant(3-Benzoylphenyl)ethanenitrileHCID 88857—
ReactantSodium ethoxideHCID 2723922—
ReactantSodiumHCID 5360545—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Product2-(3-Benzoylphenyl)-2-(hydroxyimino)acetonitrileHCID 7388434899%

Reaction Steps

To a solution of sodium ethoxide prepared from sodium (1.70 g) and ethanol (40 ml) was added dropwise a solution of 2-(3-benzoylphenyl)acetonitrile (13.6 g) in ethanol (30 ml) at 0° C., and then isoamyl nitrite (12.4 ml) was added dropwise. After stirring at room temperature for 15 hours, the reaction mixture was diluted with ethyl acetate and washed successively with 1N hydrochloric acid and an aqueous saturated solution of sodium chloride. The ethyl acetate layer was dried (MgSO4) and concentrated to obtain 2-(3-benzoylphenyl)-2-(hydroxyimino)acetonitrile (15.2 g, yield 99%) as crystals. Recrystallization from ethyl acetate-hexane gave an isomer of 2-(3-benzoylphenyl)-2-(hydroxyimino)acetonitrile as colorless crystals. m.p. 175-176° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06251926B1
Source datasetuspto-grants-2001_06
ORD IDord-7946facdf50c412a8d52b3766e30bfa4
Source noteuspto-grants-2001_06