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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767906Generated: October 31, 2026

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

https://huagongshe.com/reaction/1767906

Reaction equation

Participants

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

Reaction Steps

A solution of 5-hydroxy-indol (5 g, 38 mmol), tert-butyldimethylsilyl chloride (6.13 g, 39.4 mmol) and imidazole (5.37 g, 68.1 mmol) in DMF (50 ml) was stirred for 20 h at RT. Diethyl ether was added and the mixture was 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.) of 5-(tert-butyl-dimethyl-silanyloxy)-1H-indole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07235572B2
Source datasetuspto-grants-2007_06
ORD IDord-769ecbdc8143413c82d80853199b8825
Source noteuspto-grants-2007_06