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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1490566Generated: October 31, 2026

2-Methylindole → 2-Methyl-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole

https://huagongshe.com/reaction/1490566

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethylindoleHCID 7224—
ReagentBis(pinacolato)diboraneHCID 2733548—
Reagent3-pyridin-2-yl-2-(3-pyridin-2-yl-1H-1,3,2-benzodiazaborol-2-yl)-1H-1,3,2-benzodiazaboroleHCID 122380799—
CatalystBis(1,5-cyclooctadiene)dimethoxydiiridiumHCID 76001521—
SolventCyclopentyl methyl etherHCID 138539—
Product2-Methyl-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indoleHCID 2496059464%

Reaction Conditions

Temperature50 °C

Reaction Steps

The general procedure A was followed using 2-methyl-1H-indole (65.6 mg, 0.5 mmol.) and B2pin2 (126.9 mg, 0.5 mmol, 1.0 eq.) as starting material. The resulting mixture was allowed to stir 16 hours at 50 oC. 5y was obtained as white solid (82.3 mg, 64 %) after purification by silica gel flash chromatography (EtOAc/PE=1:40 v/v). m.p.: 73-75 oC.

Provenance & Evidence

DOI10.1021/jacs.5b05252
Source datasetBorylation dataset from Roche
ORD IDord-8a9da9cdfb524f499e336b80310520a5
Source noteBorylation dataset from Roche