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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113428Generated: October 31, 2026

Acetonitrile → HCID 16114316, compound

https://huagongshe.com/reaction/2113428

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
Reactant1,2-DimethylimidazoleHCID 15617—
Reactant1-(Chloroacetyl)pyrrolidineHCID 88440—
Solventtert-Butyl methyl etherHCID 15413—
ProductHCID 16114316HCID 1611431641%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of N-(chloroacetyl)pyrrolidine (2.0 g, 13.55 mmol) and 1,2-dimethylimidazole (1.3 g, 13.5 mmol) were heated neat at 110° C. for 3 hours. To the reaction mixture was added acetonitrile (5 mL), and heating was continued for 20 minutes. Tert-butyl methylether (10 mL) was added, and the resulting mixture was allowed to stand at room temperature overnight. The product was recovered by filtration, and washed with a mixture of tert-butyl methyl ether and acetonitrile (7:3 v/v, 50 mL). The crude product was recrystallized from a mixture of acetonitrile and tert-butyl methyl ether to obtain 1.23 g (41%) of a white solid; mp 191-193° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432254B2
Source datasetuspto-grants-2008_10
ORD IDord-902672bf16ef42799ca5dc3d3cec2f8b
Source noteuspto-grants-2008_10