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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 920116Generated: October 30, 2026

Imidazole → 4-(Tert-butyldimethylsilyl)oxy-2-nitroaniline

https://huagongshe.com/reaction/920116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant4-Amino-3-NitrophenolHCID 3758882—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product4-(Tert-butyldimethylsilyl)oxy-2-nitroanilineHCID 12042299106%

Reaction Steps

To a solution of 4-amino-3-nitrophenol (1.0 g, 6.5 mmol) and TBSCl (1.32 g, 8.8 mmol) in DMF (10 mL) was added imidazole (0.88 g, 13.0 mmol) at room temperature. The mixture was stirred at room temperature overnight. The mixture was diluted with ethyl acetate (300 mL), and washed with brine (100 mL) and dried over anhydrous sodium sulfate and concentrated. The residue was purified by silica gel chromatography (eluted with PE:EtOAc 2:1) to obtain the title compound (1.85 g, 100%) as gray solid. 1HNMR (600 MHz, CDCl3) δ 7.54 (d, J=2.7 Hz, 1H), 6.96 (dd, J=8.9, 2.7 Hz, 1H), 6.70 (d, J=8.9 Hz, 1H), 0.96 (s, 9H), 0.18 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273046B2
Source datasetuspto-grants-2016_03
ORD IDord-1d06bec6c6fb40498e809da973d9d061
Source noteuspto-grants-2016_03