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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518926Generated: October 26, 2026

Imidazole → 4-[(tert-butyldimethylsilyl)oxy]-N-phenylaniline

https://huagongshe.com/reaction/518926

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantWaterHCID 962—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant4-HydroxydiphenylamineHCID 31208—
SolventAcetonitrileHCID 6342—
Product4-[(tert-butyldimethylsilyl)oxy]-N-phenylanilineHCID 91741586—

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 12 g of 4-anilinophenol (64.7 mmol) in 200 mL of acetonitrile there are added, at ambient temperature, 6.7 g of imidazole (97.05 mmol) and 11.7 g of tert-butyl(chloro)dimethylsilane (77.64 mmol). The batch is stirred at 70° C. for 4 hours. The reaction mixture is then poured into water and extracted with ether. The organic phase is then dried over magnesium sulphate, then filtered and evaporated to dryness. The crude product thereby obtained is then purified by chromatography over silica gel (petroleum ether/dichloromethane gradient). The title product is obtained in the form of a powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115159B2
Source datasetuspto-grants-2015_08
ORD IDord-38cd0277e98c48ea9bd94c47b89a9275
Source noteuspto-grants-2015_08