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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340580Generated: October 30, 2026

Acetyl chloride → 1-Acetyl-4-methylimidazole

https://huagongshe.com/reaction/340580

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
ReactantHCID 178418800HCID 178418800—
SolventAcetonitrileHCID 6342—
Product1-Acetyl-4-methylimidazoleHCID 10953492—

Reaction Steps

To a solution of 4-methylimidazole (2.70 g, 33.0 mmol) in 10 mL of acetonitrile at 0° C. was added triethylamine (NEt3) (4.00 g, 39.6 mmol) and acetyl chloride (2.80 g, 36.3 mmol). The mixture was allowed to attain RT then filtered to remove the ppt and the filtrate was concentrated to give 1-(4-methyl-imidazol-1-yl)-ethanone, which was used without further purification in the next step. To a solution of 1-(4-methyl-imidazol-1-yl)-ethanone (4.10 g, 33.0 mmol) in 15 mL acetonitrile was added SEM-C1 (5.80 g, 35.0 mmol) and the solution was stirred at 25° C. for 10 h. The solvents were removed by evaporation and to the residue was added 100 mL of 2.5 M NaOH and the mixture was stirred at 25° C. for 1 h. The reaction mixture was then extracted with ether (3×100 mL), dried over Na2SO4 and concentrated. The title compound was purified by chromatography on silica gel eluting with 75% EtOAc/hexanes to give 4.30 g (61%) of a colorless oil: Mass spectrum (ESI, m/z): Calcd. for C10H20N2O4Si, 213.1 (M+H). found 213.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895584B2
Source datasetuspto-grants-2014_11
ORD IDord-1a481bb503ca491aba1c2720d3330d19
Source noteuspto-grants-2014_11