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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 395813Generated: October 29, 2026

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

https://huagongshe.com/reaction/395813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantDimethylformamideHCID 6228—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant4-Amino-3-NitrophenolHCID 3758882—
SolventEthyl AcetateHCID 8857—
Product4-(Tert-butyldimethylsilyl)oxy-2-nitroanilineHCID 1204229997.3%

Reaction Steps

To a mixture of 4-amino-3-nitrophenol (10.07 g, 65.3 mmol) and DMF (20 mL) was added imidazole (11.15 g, 163.8 mmol) followed by t-butyldimethylsilyl chloride (11.82 g, 78.4 mmol) in several portions. After 5 h the reaction was diluted with EtOAc (150 mL) and washed with water (5×20 mL). The organic layer was MgSO4, dried, filtered, and concentrated. The residue was chromatographed (10% EtOAc/hexanes to 20% EtOAc/hexanes) to give the title compound as a solid (17.06 g, 97%); mp 80-83° C.; IR (CHCl3): 3399, 2932, 1519, 1242, 866 cm−1; NMR (300 MHz, CDCl3): δ 0.19 (s, 6H), 0.97 (s, 9H), 6.70 (d, 1H, J=9.0), 6.95 (d, 1H, J=3.0), 7.56 (d, 1H, J=2.7); MS(FD): 268.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06605626B2
Source datasetuspto-grants-2003_08
ORD IDord-f4049c4f3069452193b8db9ff92e0aa5
Source noteuspto-grants-2003_08