Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 32917Generated: October 29, 2026

Dimethylformamide → Methyl 1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazole-4-carboxylate

https://huagongshe.com/reaction/32917

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloromethyl 2-(trimethylsilyl)ethyl etherHCID 2724271—
ReactantHCID 178418785HCID 178418785—
SolventEthyl AcetateHCID 8857—
ProductMethyl 1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazole-4-carboxylateHCID 2295404285%

Reaction Conditions

Temperature80 °C

Reaction Steps

A flask charged with 1H-imidazole-4-carboxylic acid methyl ester (0.29 g, 2.3 mmol), K2CO3 (0.60 g, 4.3 mmol), SEM-Cl (0.45 mL, 2.5 mmol) and DMF (5 mL) was heated for 12 h at 80° C. The reaction was diluted with EtOAc (20 mL) and washed with water (20 mL) and brine (20 mL) and the organic layer dried over MgSO4 and concentrated. The residue was purified by elution from a 20-g SPE cartridge (silica) with 5% MeOH/DCM to give 0.50 g (85%) of 1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazole-4-carboxylic acid methyl ester. This compound was stirred overnight at RT in MeOH (3.0 mL) and 1N NaOH (1.9 mL) and then concentrated to give 0.43 g (70%) of the title compound as a white solid. Mass spectrum (ESI), m/z): Calcd. for C10H18N2O3Si, 243.1 (M+H), found 243.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07427683B2
Source datasetuspto-grants-2008_09
ORD IDord-dccf4a15551a4974a2d2e06620359aa8
Source noteuspto-grants-2008_09