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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768459Generated: October 31, 2026

Imidazole → HCID 58638077, compound

https://huagongshe.com/reaction/1768459

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantEthyl AcetateHCID 8857—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantHCID 23614741HCID 23614741—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
SolventSodium HydroxideHCID 14798—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 58638077HCID 58638077—

Reaction Conditions

Temperature60 °C

Reaction Steps

A suspension of 1.75 g (5.6 mmol) 1-7 in 15 mL of EtOH and 10 mL of 3 M NaOH was heated at 60° C. for 3 h, cooled to room temperature and dumped into a separatory funnel with EtOAc and brine. The layers were separated, the aqueous phase was extracted twice with EtOAc, the combined organic phases were washed twice with brine, dried over Na2SO4, and concentrated to provide a white solid. To this flask was added 30 mL of CH2Cl2, 1.5 g (22.3 mmol) of imidazole and 1.76 g (11.7 mmol) of TBSCl, and the resultant suspension was stirred overnight. The reaction was diluted with CH2Cl2, washed twice with water, dried over Na2SO4, concentrated, and the residue purified by silica gel chromatography with EtOAc/hexanes to provide 1-8 as a white solid. Data for 1-8: 1HNMR (500 MHz, CDCl3) δ 7.6-7.3 (m, 5H), 7.1-6.9 (m, 3H), 6.75 (s, 1H), 4.25 (d, 1H), 4.1 (d, 1H), 3.95 (d, 1H), 3.75 (d, 1H), 0.9 (s, 9H), 0.1 (s, 3H), 0.05 (s, 3H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07235580B2
Source datasetuspto-grants-2007_06
ORD IDord-bab1358b8c224a42b4a64a3ec234ac60
Source noteuspto-grants-2007_06