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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213067Generated: October 31, 2026

Imidazole → HCID 66739120, compound

https://huagongshe.com/reaction/2213067

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-ButyldiphenylchlorosilaneHCID 94078—
Reactant(S)-(+)-gamma-Hydroxymethyl-gamma-butyrolactoneHCID 2733813—
SolventDimethylformamideHCID 6228—
ProductHCID 66739120HCID 6673912097%

Reaction Steps

To a solution of 3 (7.0 g, 60 mmol) and imidazole (9.19 g, 135 mmol) in anhydrous DMF (70 mL) was added tert-butyldiphenylsilyl chloride (18.14 g, 66 mmol, 17.2 mL), and the solution was stirred at room temperature under a nitrogen atmosphere for 1 h. After removal of the solvent by evaporation, the residue was dissolved in CHCl3, washed with water and brine, dried (Na2SO4), filtered, and concentrated. After crystallization from hexane, the oily residue gave the title compound 4 as a white crystalline solid (20.6 g, 97%). M.P. 76° C.; 1H NMR (CDCl3) δ7.68–7.65 (m, 4H, arom.), 7.47–7.39 (m, 6H, arom.), 4.63–4.61 (m, 1H, H-5), 3.90–3.87 (dd, J=3 & 11 Hz, 1H, CH2OH), 3.70–3.67 (dd, J=3 & 11 Hz, 1H, CH2OH), 2.69–2.65 (m, 1H, H-3), 2.56–2.52 (m, 1H, H-3), 2.32–2.23 (m, 2H, H-4), 1.06 (s, 9H, t-Bu).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105527B2
Source datasetuspto-grants-2006_09
ORD IDord-974edaaeace24eeb8e37a225d258f7c0
Source noteuspto-grants-2006_09