Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 48133Generated: October 26, 2026

Water → 2-Methylsulfonyloxyimino-4-(4-methoxy-phenyl)-but-3-enenitrile

https://huagongshe.com/reaction/48133

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant2-Hydroxyimino-4-(4-methoxy-phenyl)-but-3-enenitrileHCID 86759358—
SolventTetrahydrofuranHCID 8028—
Product2-Methylsulfonyloxyimino-4-(4-methoxy-phenyl)-but-3-enenitrileHCID 5452275141%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-hydroxyimino-4-(4-methoxy-phenyl)-but-3-enenitrile (1.8 g; 9 mmol) is dissolved in 15 ml of anhydrous tetrahydrofuran, and cooled to 0° C. Methanesulfonyl chloride (0.93 ml, 0.012 mol) is added at once, followed by triethylamine (2 ml, 0.015 mol) dropwise over 20 min, keeping the temperature of the mixture below 5° C. The mixture is then stirred at 2° C. for 1 h 15 min, and poured into 200 ml of iced water. The suspension is extracted with ethyl acetate, the organic extract is washed neutral with water, then with brine, and dried over magnesium sulfate. Rotary evaporation of the solvent and recrystallization from 80 ml of ethanol yields 2-methylsulfonyloxyimino-4-(4-methoxy-phenyl)-but-3-enenitrile (1.02 g; 41%) as light yellow hair-like crystals, mp 147-152° C. (dec). 1H-NMR reveals the presence of only one isomer.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06703182B1
Source datasetuspto-grants-2004_03
ORD IDord-212d808d04a24f93b79c9b42fc64dcf5
Source noteuspto-grants-2004_03