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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 506641Generated: October 31, 2026

Imidazole → 5-(tert-butyl-dimethyl-silanyloxy)-1H-indole-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/506641

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantAmmonium ChlorideHCID 25517—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant5-Hydroxyindole-2-carboxylic acidHCID 88958—
SolventDimethylformamideHCID 6228—
Product5-(tert-butyl-dimethyl-silanyloxy)-1H-indole-2-carboxylic acid ethyl esterHCID 2267673098.5%

Reaction Steps

To the solution of 10.0 g (49.0 mmol) 5-hydroxyindole-2-carboxylic acid (commercially available) in 30 ml N,N-dimethylformamide, 7.7 g (51.1 mmol) tert-butyldimethylchlorosilane and 3.5 g (51.4 mmol.) imidazole was added. After 1 hour, the solution was poured on 10% aqueous ammonium chloride solution and was extracted three times with ethyl acetate. The combined organic layers were washed with brine, dried over magnesium sulfate, filtered and evaporated. The residue was purified by column chromatography over silica gel with ethyl acetate:n-hexane (1:2 v/v) as eluant to give 15.3 g (98.5%) of the compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786109B2
Source datasetuspto-grants-2010_08
ORD IDord-15dc94ec6bab4687b98ddb49bb8a8b64
Source noteuspto-grants-2010_08