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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2042332Generated: November 1, 2026

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

https://huagongshe.com/reaction/2042332

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, 1H) and 8.34 (m, 1H). MS (ES+): m/z 176.15 [MH+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586546B2
Source datasetuspto-grants-2013_11
ORD IDord-0aa7e8e04c01453aa70604edd088e350
Source noteuspto-grants-2013_11