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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 550165Generated: October 25, 2026

Methyl iodide → (1-Methyl-1H-indol-6-yl)boronic acid

https://huagongshe.com/reaction/550165

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
Reactant1H-Indol-6-ylboronic acidHCID 2763205—
Product(1-Methyl-1H-indol-6-yl)boronic acidHCID 21709054—

Reaction Steps

A mixture of indole-6-boronic acid (0.100 g, 0.615 mmol), sodium hydride (0.07 g, 20 mmol) and THF (5 mL, 60 mmol) was stirred at rt for 20 min. then methyl iodide (100 uL, 20 mmol) was added and the mixture was allowed ro stir at rt for 3 hours. The reaction was quenched with sat. NH4Cl solution, washed with brine and dried over Na2SO4, then the solvent was removed in vacuo. The crude product was purified by chromatography over silica gel eluting with 1:9 EtOAc/hexane and 1% MeOH, yielding the desired product. 1H NMR (400 MHz, CDCl3) δ ppm 3.99 (s, 3H), 6.58 (m, 1H). 7.23 (m, 1H), 7.81 (m, 1H), 8.08 (m, IH) and 8.34 (m, 1H). MS (ES+): m/z 176.15 [MH+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943767B2
Source datasetuspto-grants-2011_05
ORD IDord-2001d092655246278750901c838f0880
Source noteuspto-grants-2011_05