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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16567Generated: October 26, 2026

Imidazole → 4-(t-Butyldimethylsilyloxy)indole

https://huagongshe.com/reaction/16567

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant1H-indol-4-olHCID 75421—
SolventDichloromethaneHCID 6344—
Product4-(t-Butyldimethylsilyloxy)indoleHCID 11593976113.3%

Reaction Steps

A solution of 4-hydroxyindole (13.31 g, 75 mmol) in dry dichloromethane (400 mL) was treated with imidazole (8.17 g, 120 mmol) and t-butyldimethylsilyl chloride (18.09 g, 120 mmol) and the mixture was stirred at room temperature under nitrogen overnight. The precipitated white solid was filtered off and washed with dichloromethane and the combined filtrates were washed successively with 0.5 M aq. hydrochloric acid, 0.5 M aq. sodium hydroxide and brine, dried and evaporated to give 9 as white crystals (21.03 g, 85%), mp 80-81° C. (from hexanes); 1H NMR (500 MHz) δ 8.06 (br s, 1H), 7.08 (dd, J=3.1, 2.4 Hz, 1H), 6.99-7.05 (m, 2H), 6.58-6.59 (m, 1H), 6.52 (dd, J=7, 1.5 Hz, 1H, 1.06 (s, 9H), 0.23 (s, 6H). Anal. Calcd. for C14H21NOSi: C, 67.97; H, 8.56; N, 5.66. Found: C, 67.60; H, 8.80; N, 5.57.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737169B2
Source datasetuspto-grants-2010_06
ORD IDord-cafe1f939f3a4c769dbba9559b0274bf
Source noteuspto-grants-2010_06