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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1870511Generated: October 30, 2026

Diethyl Sulfate → HCID 15457414, compound

https://huagongshe.com/reaction/1870511

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-vinyldicyanoimidazole. 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 numberUS06096899
Source datasetuspto-grants-2000_08
ORD IDord-bef51d949b9a4ae9ad82da927ccb9266
Source noteuspto-grants-2000_08