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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2116725Generated: November 1, 2026

Imidazole → HCID 68949735, compound

https://huagongshe.com/reaction/2116725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant6-Hydroxy-1H-indole-2-carboxylic acidHCID 22350191—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68949735HCID 6894973590.1%

Reaction Steps

6-Hydroxy-1H-indole-2-carboxylic acid (5.40 g, 30.48 mmol) is dissolved in THF (100 ml) and imidazole (10.38, 152.4 mmol) is added. The mixture is stirred for 5 minutes, TBDMS-Cl (13.78 g, 91.44 mmol) is added. The reaction is stirred at room temperature for 1 hour. The mixture is filtered into water (200 ml). The solid is washed with THF (50 ml). The filtrate is concentrated to remove THF. The product is extracted with ethyl acetate (100 ml) three times. The organic is dried (MgSO4), filtered, and concentrated to provide 6-(tert-Butyl-dimethyl-silanyloxy)-1H-indole-2-carboxylic acid (8.0 g, 90% yield). 1H NMR (400 MHz, DMSO-d6): δ 12.73 (s, 1H) , 11.43 (s, 1H), 7.49 (d, 1H), 7.00 (s, 1H), 6.84 (s, 1H), 6.63 (m, 1H), 0.97 (s, 9H), 0.20 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07439249B2
Source datasetuspto-grants-2008_10
ORD IDord-00cb47dc47c048ecbd80264e0849eb3e
Source noteuspto-grants-2008_10