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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922632Generated: November 1, 2026

Acetonitrile → HCID 86719632, compound

https://huagongshe.com/reaction/922632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantButyl bromideHCID 8002—
ReactantPotassium HydroxideHCID 14797—
Reactant1-(2-Bromoethyl)naphthaleneHCID 139541—
Reactant4,5-DichloroimidazoleHCID 140018—
ReactantPotassium BromideHCID 253877—
ProductHCID 86719632HCID 86719632—

Reaction Steps

4,5-Dichloroimidazole (1.23 g, 9 mmol) will be dissolved into acetonitrile. Potassium hydroxide (0.61 g, 9.9 mmol) will be added and the mixture will be allowed to stir for 0.5 h. 1-bromobutane (9 mmol) will be added and the solution will be allowed to reflux overnight. The solution will be filtered hot to remove a white precipitate (presumed to be KBr) and 1-(2-bromoethyl)naphthalene (9 mmol) will be added and the mixture will be returned to reflux overnight. The mixture will be allowed to cool to room temperature, and the volatiles will be removed en vacuo resulting in the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278951B2
Source datasetuspto-grants-2016_03
ORD IDord-8b60f9917d774b9981233fa655e01bba
Source noteuspto-grants-2016_03