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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047872Generated: October 31, 2026

Acetonitrile → HCID 87508268, compound

https://huagongshe.com/reaction/1047872

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantPotassium CarbonateHCID 11430—
Reactant1,2-Bis(bromomethyl)-4,5-dichlorobenzeneHCID 291142—
ReactantEthyl isocyanoacetateHCID 533707—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
ProductHCID 87508268HCID 8750826866%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of ethyl isocyanoacetate (3.85 mL, 35 mmol) in anhydrous ACN (300 mL) is added finely ground anhydrous K2CO3 (29 g, 210 mmol), TBAHS (tetrabutyl ammonium hydrogen sulfate, 2.34 g, 7 mmol), and 1,2-bis-(bromomethyl)-4,5-dichlorobenzene (11.6 g, 35 mmol). The resulting heterogeneous mixture is stirred at 80° C. overnight. The reaction mixture is cooled down to RT and filtered to remove the unwanted salts. The filtrate is concentrated in vacuo. The residue is purified by flash column chromatography (200 g silica gel; gradient elution: 0-25% EtOAc in heptane) to give a pure product as white powder (6.63 g, 66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569535B2
Source datasetuspto-grants-2013_10
ORD IDord-70eaa245bb7e4c2dba55b25f5bc813ce
Source noteuspto-grants-2013_10