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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 567965Generated: October 29, 2026

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

https://huagongshe.com/reaction/567965

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant2-Amino-5-NitrophenolHCID 4984721—
SolventDimethylformamideHCID 6228—
Product2-[(Tert-butyldimethylsilyl)oxy]-4-nitroanilineHCID 1548571098%

Reaction Conditions

Temperature23 °C

Reaction Steps

To a solution of 2-amino-5-nitrophenol (1 g, 6.49 mmol) and imidazole (0.88 g, 12.3 mmol) in DMF (15 mL), tert-butyldimethylsilyl chloride (11.2 mL, 64.9 mmol) was added. The resulting mixture was allowed to stir at 23° C. for 48 hours. The reaction mixture was partitioned between 0.1% HCl and ethyl acetate. The combined organic phase was washed with brine, dried over MgSO4 and filtered. Removal of solvent at reduced pressure and chromatography of the resulting oil on silica gel (hexane:ethyl acetate; 5:1) gave the tided compound (1.7 g, 98%). 1H NMR (CDCl3): δ 7.78 (dd, 1H, J=6.7 Hz and J=2.7 Hz), 7.61 (d, 1H, J=2.7 Hz), 6.7 (d, 1H, J=8.8 Hz), 1.0 (s, 9H), 0.28 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06180675B2
Source datasetuspto-grants-2001_01
ORD IDord-e5a6415363fa4807aab7dd132367a52d
Source noteuspto-grants-2001_01