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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018775Generated: October 30, 2026

Dimethyl Sulfate → HCID 12113162, compound

https://huagongshe.com/reaction/1018775

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfateHCID 6497—
Reactant2-Ethenyl-1H-imidazole-4,5-dicarbonitrileHCID 12113161—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 12113162HCID 1211316252.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 0.602 g (4.17 mmol) of 2-vinyl-4,5-dicyanoimidazole in distilled THF (15 mL) at 0° C. under nitrogen was added slowly while stirring 0.22 mL (2.32 mmol) of dimethyl sulfate and 0.60 mL (4.30 mmol) triethylaminine via syringe. The reaction solution was allowed to come to room temperature and was stirred for 15 hours. The reaction solution was concentrated down under a stream of nitrogen and dissolved in 10 mL CH2Cl2. This solution was washed twice with a 10% solution of NaOH and twice with a saturated solution of NaCl. CH2Cl2 was stripped off, leaving a brown oil. This oil was dissolved in approximately 1 mL of THF and precipitated out in hexane. The precipitate was vacuum filtered and dried to yield 0.345 g (52.4% yield) of a light brown, fluffy powder. This powder was dissolved in 100 mL of ether and vacuum filtered to remove undissolved particles. 20 mL of hexane was added to the ether solution, and the solution was cooled to 0° C. White, needle-shaped crystals were formed and vacuum filtered.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06482954B2
Source datasetuspto-grants-2002_11
ORD IDord-ee1ba16c6a8149b5a50fc3a47ca7d636
Source noteuspto-grants-2002_11