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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 574750Generated: October 30, 2026

Imidazole → HCID 10477824, compound

https://huagongshe.com/reaction/574750

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantSulfuric AcidHCID 1118—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant1-O-HexadecylglycerolHCID 72733—
SolventPyridineHCID 1049—
ProductHCID 10477824HCID 10477824100%

Reaction Steps

Compound 2a (2.297 g, 7.26 mmol) was dissolved in anhydrous pyridine (20 mL) at RT under argon. Imidazole (1.02 g, 14.52 mmol) in anhydrous pyridine (10 mL) was then added followed by tert-butyl dimethylsilyl chloride (TBDMS-Cl, 2.25 g, 14.52 mmol) in anhydrous pyridine (20 mL). The reaction mixture was stirred at RT for 72 hours, poured into 0.5 M H2SO4 (150 mL) and extracted with diethyl ether (100 mL, 3×). The extract was washed successively with saturated aqueous NaHCO3 (100 mL) and water (100 mL), dried over anhydrous Na2SO4 and the solvent removed under reduced pressure to obtain 3a, an oily material which was dried in a vacuum dessicator for 2 days (3.164 g, 100% yield). 1H NMR (in CDCl3): δ in ppm 0.83-0.89 (15H, m), 1.22 (29H, m), 1.52-1.53 (2H, m), 2.60 (1H, s, D2O exchangeable), 3.40-3.42 (4H, m), 3.59-3.61 (2H, m), 3.64 (1H, m); 13C NMR (in CDCl3): δ in ppm 14.3, 18.2, 18.5, 22.9, 25.8, 26.0, 26.1, 26.3, 29.6, 29.8, 29.9, 32.1, 33.0, 64.2, 70.8, 71.6, 71.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034923B2
Source datasetuspto-grants-2015_05
ORD IDord-c9964f5d9b764149983f561c9170b442
Source noteuspto-grants-2015_05