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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 893548Generated: October 26, 2026

5,6-Dihydroxyindole → Di(trimethylsilyloxy]indole

https://huagongshe.com/reaction/893548

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5,6-DihydroxyindoleHCID 114683—
ReactantN,O-bis(trimethylsilyl)acetamideHCID 6913588—
SolventDichloromethaneHCID 6344—
ProductDi(trimethylsilyloxy]indoleHCID 13171743471%

Reaction Steps

To 0.81 g (0.004 mole) of N,O-bis(trimethylsilyl) acetamide is added, stirring at room temperature, 0.3 g (0.002 mole) of 5,6-dihydroxy indole. When dissolution is completed, 2 ml dichloromethane are added and the solution is passed through a column of silica 60, eluating with dichloromethane. The first fraction obtained is concentrated in a rotavapor, then vacuum-dried. Thus are obtained 0.42 g (yield: 71%) of white crytal of 5,6[di(trimethylsilyloxy]indole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05126125
Source datasetuspto-grants-1992_06
ORD IDord-4e923568dff24e089cee1cc2d5e733ab
Source noteuspto-grants-1992_06