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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1779723Generated: November 1, 2026

Dimethyl Sulfate → HCID 54390956, compound

https://huagongshe.com/reaction/1779723

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfateHCID 6497—
ReactantButyl nitriteHCID 10996—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 11118528HCID 11118528—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 54390956HCID 5439095687.7%

Reaction Steps

95% Sodium hydroxide (0.32 g, 7.5 mmol), acetone (5 ml) and butyl nitrite (0.62 g, 6 mmol) were added to 2-(2,5dimethylphenoxymethyl)benzyl cyanide (1.26 g, 5 mmol). The mixture was stirred at room temperature for 2 hours. Dimethyl sulfate (0.95 g, 7.5 mmol) was added, and the mixture was stirred under ice-cooling for 10 minutes and at room temperature for 1 hour. After completion of the reaction, toluene (10 ml) and 1N aqueous sodium hydroxide solution (10 ml) were added, and the mixture was stirred at room temperature for 1 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-(2,5-dimethylphenoxy-methyl)-α-methoxyiminobenzyl cyanide (1.29 g, Yield: 87.6%, E/Z=13/87).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05627284
Source datasetuspto-grants-1997_05
ORD IDord-fe7a20c1d7dd40acabc58a3a5bffe6c9
Source noteuspto-grants-1997_05