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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018776Generated: October 31, 2026

Diethyl Sulfate → HCID 15457414, compound

https://huagongshe.com/reaction/1018776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl SulfateHCID 6163—
ReactantTriethylamineHCID 8471—
Reactant2-Ethenyl-1H-imidazole-4,5-dicarbonitrileHCID 12113161—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
SolventEthyl acetate hexaneHCID 21226206—
ProductHCID 15457414HCID 1545741465%

Reaction Steps

A flask equipped with a magnetic stirbar was charged with 6.26 g of 2-vinyidicyanoimidazole. To this, 75 ml of distilled THF and 6.1 ml of triethylamine were added with stirring. After 5 minutes stirring, 5.7 ml of diethyl sulphate was added. This mixture was allowed to stir for 2 days. Analysis by TLC (50/50 hexane/ethyl acetate, UV visualization) showed the reaction was complete (starting material rf 0.3, product rf 0.6). The THF solution was rotovapped and the residue was dissolved in ethyl acetate. The ethyl acetate was washed with 10% aqueous sodium hydroxide. The combined aqueous layers were back extracted with methylene chloride. The combined organic layers were dried with magnesium sulphate and rotovapped to dryness. The crude residue was triturated with ether. The ether extracts were rotovapped and the residue recrystallized with ether/hexanes to yield 3.124 g of the product, mp 66-70° C. as yellow needles. A second crop yielded 1.72 g for a combined yield of 65%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06482954B2
Source datasetuspto-grants-2002_11
ORD IDord-cf5e280a241246df8223568f2d0c671e
Source noteuspto-grants-2002_11