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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272874Generated: October 26, 2026

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

https://huagongshe.com/reaction/2272874

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
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 whole is stirred at 70° C. for 4 hours. Then the reaction mixture is poured onto water and extracted with ether. The organic phase is subsequently dried over magnesium sulphate and then filtered and evaporated to dryness. The crude product so 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 numberUS09120791B2
Source datasetuspto-grants-2015_09
ORD IDord-edca8ab8877c4e4ab290ed85435d8919
Source noteuspto-grants-2015_09