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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2065055Generated: October 31, 2026

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

https://huagongshe.com/reaction/2065055

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 numberUS08288419B2
Source datasetuspto-grants-2012_10
ORD IDord-da714cb1aa684ec0b719b3d38c164df4
Source noteuspto-grants-2012_10