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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993240Generated: November 2, 2026

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

https://huagongshe.com/reaction/1993240

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 numberUS07651687B2
Source datasetuspto-grants-2010_01
ORD IDord-8fa412b1efb7408d944f406759fae38b
Source noteuspto-grants-2010_01