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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42827Generated: October 29, 2026

Imidazole → 2-[1-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-oxazole

https://huagongshe.com/reaction/42827

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantNitrogenHCID 947—
ReactantAmmonium ChlorideHCID 25517—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant1-(Oxazol-2-yl)ethanolHCID 21942786—
SolventTetrahydrofuranHCID 8028—
Product2-[1-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-oxazoleHCID 66821548—

Reaction Steps

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), 1-oxazol-2-yl-ethanol (348 mg, 3.08 mmol) was dissolved in dry THF (15 mL). tert-Butyldimethylsilyl chloride (580 mg, 3.85 mmol) was added at rt followed by imidazole (262 mg, 3.85 mmol). The reaction mixture was stirred at rt for 16 h. Sat. aq. NH4Cl (20 mL) was added, the layers separated and the aq. layer extracted with EA (2×20 mL). The combined org. extracts were dried over MgSO4, filtered, and the solvent removed under reduced pressure. Purification of the residue by FC (1:4 Et2O-hexane) gave the title compound as a colorless oil. TLC:rf (1:4 Et2O-hexane)=0.39. LC-MS-conditions 02: tR=1.08 min, [M+H]+=228.48

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536209B2
Source datasetuspto-grants-2013_09
ORD IDord-fa383d1a4c1b4a2dba9e4c72e3afc6dd
Source noteuspto-grants-2013_09