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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1779729Generated: November 1, 2026

Dimethyl Sulfate → 2-Phenoxy-alpha-methoxyiminobenzyl cyanide

https://huagongshe.com/reaction/1779729

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfateHCID 6497—
ReactantButyl nitriteHCID 10996—
ReactantSodium HydroxideHCID 14798—
Reactant2-PhenoxyphenylacetonitrileHCID 141221—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product2-Phenoxy-alpha-methoxyiminobenzyl cyanideHCID 5416536593.6%

Reaction Steps

95% sodium hydroxide (0.40 g, 6 mmol), acetone (10 ml) and butyl nitrite (0.62 g, 6 mmol) were added to 2-phenoxybenzyl cyanide (1.05 g, 5 mmol). The mixture was stirred at room temperature for 1.5 hours. Dimethyl sulfate (0.76 g, 6 mmol) was added, and the mixture was stirred at room temperature for 0.5 hours. After completion of the reaction, ether (10 ml) and 1N aqueous sodium hydroxide solution (10 ml) were added, and the mixture was stirred at room temperature for 0.5 hour. After stirring, water (100 ml) was added. The mixture was extracted with ether (100 ml), dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The resulting residue was purified by silica gel chromatography (ethyl acetate/n-hexane) to give 2-phenoxy-α-methoxyiminobenzyl cyanide (1.18 g, Yield: 93.5%, E/Z=23/77).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05627284
Source datasetuspto-grants-1997_05
ORD IDord-80bab92854fb4f14a252ad4f959b7944
Source noteuspto-grants-1997_05