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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767958Generated: November 4, 2026

Imidazole → 5-(tert-Butyldimethylsilyloxy)-1H-indole

https://huagongshe.com/reaction/1767958

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactant5-HydroxyindoleHCID 16054—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product5-(tert-Butyldimethylsilyloxy)-1H-indoleHCID 22250817100%

Reaction Steps

A suspension of 5-hydroxy-indol (5 g, 38 mmol), tert-butyldimethylsilyl chloride (6.1 g, 39.4 mmol) and imidazole (5.4 g, 68 mmol) in DMF (50 ml) was stirred for 20 h at RT. The reaction mixture was taken up in ether and washed with 1N HCl and water. The organic layer was dried over sodium sulfate and concentrated under reduced pressure to give 9.4 g (38 mmol, quant.) 5-(tert-butyl-dimethyl-silanyloxy)-1H-indole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07235572B2
Source datasetuspto-grants-2007_06
ORD IDord-0239daa7befe4aee80832a33a78985d1
Source noteuspto-grants-2007_06